A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974588



Internal ID18609799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:65806648..65817467hg38UCSC Ensembl
Innerchr15:66098986..66109805hg19UCSC Ensembl
Innerchr15:63886040..63896859hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3810820
hg1910820
hg1810820
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2028851, nssv2028850, nssv2028847, nssv2028856, nssv2028849, nssv2028854, nssv2028853, nssv2028852, nssv2028855, nssv2028848
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)nsv974588
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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