A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437346



Internal ID15036078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:223716893..223717318hg38UCSC Ensembl
Outerchr1:223716079..223717830hg38UCSC Ensembl
Innerchr1:223904595..223905020hg19UCSC Ensembl
Outerchr1:223903781..223905532hg19UCSC Ensembl
Innerchr1:221971218..221971643hg18UCSC Ensembl
Outerchr1:221970404..221972155hg18UCSC Ensembl
Innerchr1:220879226..220879651hg16UCSC Ensembl
Outerchr1:220878412..220880163hg16UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg381752
hg191752
hg181752
hg161752
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv467227
SamplesNA10856
Known GenesCAPN2
MethodSNP array
AnalysisOur algorithm aims to detect deletions that are transmitted from a hemizygous parent to a child. For each trio, every SNP was coded into one of seven categories: (A) Type I mendelian incompatibility (that is, consistent with deletion) involving mother; (B) Type I mendelian incompatibility involving father; (C) Type II mendelian incompatibility (that is, inconsistent with deletion); (D) child homozygous or missing data, both parents homozygous or missing data; (E) child homozygous or missing data, father heterozygous, mother homozygous or missing data; (F) child homozygous or missing data, mother heterozygous, father homozygous or missing data; (G) child heterozygous or both parents heterozygous (see Supplementary Methods for further details). SNPs were assigned to states D-G only if they did not contain mendelian incompatibilities. A run of consecutive SNPs in a particular trio was considered to be consistent with a maternal transmitted deletion if all SNPs were in states A, D or E, or with a paternal deletion if all SNPs were in states B, D or F.
PlatformNot reported
Comments
ReferenceConrad_et_al_2006
Pubmed ID16327808
Accession Number(s)nsv437346
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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