A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970586



Internal ID18605808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:141801970..141805495hg38UCSC Ensembl
Innerchr7:141501770..141505295hg19UCSC Ensembl
Innerchr7:141148239..141151764hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg383526
hg193526
hg183526
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2481718, nssv2481721, nssv2481723, nssv2481720, nssv2481717, nssv2481722, nssv2481724, nssv2481715, nssv2481719, nssv2481716
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)nsv970586
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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