A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039708



Internal ID19128927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20359322..20411461hg38UCSC Ensembl
Innerchr15:20564575..20616714hg19UCSC Ensembl
Innerchr15:18824589..18876728hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3852140
hg1952140
hg1852140
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2260n100
Supporting Variantsnssv3537513, nssv3537510, nssv3537508, nssv3537515, nssv3537507, nssv3537512, nssv3537506, nssv3537514, nssv3537511, nssv3713777, nssv3537509
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)nsv1039708
Frequency
Sample Size11257
Observed Gain7
Observed Loss4
Observed Complex0
Frequencyn/a


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