A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981581



Internal ID18616778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:131658319..131662544hg38UCSC Ensembl
Innerchr7:131343078..131347303hg19UCSC Ensembl
Innerchr7:130993618..130997843hg18UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg384226
hg194226
hg184226
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2476864, nssv2476863, nssv2476860, nssv2476866, nssv2476861, nssv2476865, nssv2476859, nssv2476857, nssv2476862, nssv2476858
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)nsv981581
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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