A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035171



Internal ID19124390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20359322..20418941hg38UCSC Ensembl
Innerchr15:20564575..20624194hg19UCSC Ensembl
Innerchr15:18824589..18884208hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3859620
hg1959620
hg1859620
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2251n100
Supporting Variantsnssv3537516, nssv3537520, nssv3537519, nssv3537517, nssv3537521, nssv3537518
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)nsv1035171
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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