A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977682



Internal ID18612888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28192350..28198679hg38UCSC Ensembl
Innerchr15:28437496..28443825hg19UCSC Ensembl
Innerchr15:26111091..26117420hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg386330
hg196330
hg186330
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2010458, nssv2010460, nssv2010464, nssv2010467, nssv2010465, nssv2010459, nssv2010463, nssv2010461, nssv2010466, nssv2010462
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHERC2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977682
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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