A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516378



Internal ID15443671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:94252429..94257220hg38UCSC Ensembl
Innerchr15:94795658..94800449hg19UCSC Ensembl
Innerchr15:92596662..92601453hg18UCSC Ensembl
Innerchr15:92596662..92601453hg17UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg384792
hg194792
hg184792
hg174792
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv688793, nssv684399, nssv685042, nssv667915
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516378
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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