A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970833



Internal ID18606055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:55606139..55614233hg38UCSC Ensembl
Innerchr7:55673832..55681926hg19UCSC Ensembl
Innerchr7:55641326..55649420hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg388095
hg198095
hg188095
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2448502, nssv2448497, nssv2448498, nssv2448495, nssv2448500, nssv2448504, nssv2448503, nssv2448501, nssv2448496, nssv2448499
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)nsv970833
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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