A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970554



Internal ID18259090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:97860050..97871380hg38UCSC Ensembl
Innerchr7:97489362..97500692hg19UCSC Ensembl
Innerchr7:97327298..97338628hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3811331
hg1911331
hg1811331
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2469405, nssv2469402, nssv2469408, nssv2469401, nssv2469410, nssv2469409, nssv2469407, nssv2469406, nssv2469404, nssv2469403
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesASNS
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970554
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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