A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052407



Internal ID19141626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20376297..20422227hg38UCSC Ensembl
Innerchr15:20581550..20627480hg19UCSC Ensembl
Innerchr15:18841564..18887494hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3845931
hg1945931
hg1845931
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2272n100
Supporting Variantsnssv3535931, nssv3535933, nssv3535925, nssv3535928, nssv3535929, nssv3535932, nssv3535927, nssv3535926, nssv3535930, nssv3535924
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)nsv1052407
Frequency
Sample Size11257
Observed Gain7
Observed Loss3
Observed Complex0
Frequencyn/a


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