A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977664



Internal ID18612870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22494823..22497301hg38UCSC Ensembl
Innerchr15:23375795..23378273hg19UCSC Ensembl
Innerchr15:20927236..20929714hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg382479
hg192479
hg182479
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2007039, nssv2007032, nssv2007033, nssv2007038, nssv2007036, nssv2007037, nssv2007031, nssv2007030, nssv2007034, nssv2007035
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHERC2P2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977664
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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