A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974524



Internal ID18609735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22570272..22573474hg38UCSC Ensembl
Innerchr15:23299622..23302824hg19UCSC Ensembl
Innerchr15:20851063..20854265hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg383203
hg193203
hg183203
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2007553, nssv2007550, nssv2007552, nssv2007554, nssv2007555, nssv2007548, nssv2007549, nssv2007556, nssv2007551, nssv2007547
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)nsv974524
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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