A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036122



Internal ID19125341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380825..20418941hg38UCSC Ensembl
Innerchr15:20586078..20624194hg19UCSC Ensembl
Innerchr15:18846092..18884208hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3838117
hg1938117
hg1838117
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2275n100
Supporting Variantsnssv3538658, nssv3538659
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)nsv1036122
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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