A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437173



Internal ID15035905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:27159610..27164848hg38UCSC Ensembl
Outerchr15:27153403..27171221hg38UCSC Ensembl
Innerchr15:27404757..27409995hg19UCSC Ensembl
Outerchr15:27398550..27416368hg19UCSC Ensembl
Innerchr15:24987503..24992741hg18UCSC Ensembl
Outerchr15:24981296..24999114hg18UCSC Ensembl
Innerchr15:24967522..24972760hg16UCSC Ensembl
Outerchr15:24961315..24979133hg16UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3817819
hg1917819
hg1817819
hg1617819
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv467054
SamplesNA10851
Known GenesGABRG3
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)nsv437173
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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