A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970805



Internal ID18606027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:23365455..23366065hg38UCSC Ensembl
Innerchr7:23405074..23405684hg19UCSC Ensembl
Innerchr7:23371599..23372209hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38611
hg19611
hg18611
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2438657, nssv2438658, nssv2438656, nssv2438660, nssv2438662, nssv2438655, nssv2438664, nssv2438663, nssv2438659, nssv2438661
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesIGF2BP3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970805
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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