A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046679



Internal ID19135898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20381480..20512131hg38UCSC Ensembl
Innerchr15:20586733..20717374hg19UCSC Ensembl
Innerchr15:18846747..18977388hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38130652
hg19130642
hg18130642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2265n100
Supporting Variantsnssv3538712, nssv3714747
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046679
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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