A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976904



Internal ID18612110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28250206..28257129hg38UCSC Ensembl
Innerchr15:28495352..28502275hg19UCSC Ensembl
Innerchr15:26168947..26175870hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg386924
hg196924
hg186924
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2011231, nssv2011237, nssv2011228, nssv2011235, nssv2011229, nssv2011233, nssv2011230, nssv2011234, nssv2011236, nssv2011232
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)nsv976904
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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