A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976920



Internal ID18612126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:35121193..35124561hg38UCSC Ensembl
Innerchr15:35413394..35416762hg19UCSC Ensembl
Innerchr15:33200686..33204054hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg383369
hg193369
hg183369
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2018800, nssv2018804, nssv2018801, nssv2018808, nssv2018802, nssv2018805, nssv2018807, nssv2018806, nssv2018799, nssv2018803
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976920
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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