A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977647



Internal ID18612853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20504546..20511147hg38UCSC Ensembl
Innerchr15:20709799..20716390hg19UCSC Ensembl
Innerchr15:18969813..18976404hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg386602
hg196592
hg186592
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2003837, nssv2003838, nssv2003835, nssv2003839, nssv2003833, nssv2003832, nssv2003834, nssv2003840, nssv2003841, nssv2003836
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHERC2P3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977647
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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