A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437193



Internal ID15382499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:25361301..25361819hg38UCSC Ensembl
Outerchr22:25360707..25362823hg38UCSC Ensembl
Innerchr22:25757268..25757786hg19UCSC Ensembl
Outerchr22:25756674..25758790hg19UCSC Ensembl
Innerchr22:24087268..24087786hg18UCSC Ensembl
Outerchr22:24086674..24088790hg18UCSC Ensembl
Innerchr22:24081822..24082340hg16UCSC Ensembl
Outerchr22:24081228..24083344hg16UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg382117
hg192117
hg182117
hg162117
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv467074
SamplesNA12707
Known GenesLRP5L
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)nsv437193
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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