A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970799



Internal ID18606021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:15700106..15704930hg38UCSC Ensembl
Innerchr7:15739731..15744555hg19UCSC Ensembl
Innerchr7:15706256..15711080hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg384825
hg194825
hg184825
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2437782, nssv2437781, nssv2437787, nssv2437783, nssv2437784, nssv2437789, nssv2437785, nssv2437788, nssv2437786, nssv2437790
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)nsv970799
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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