A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971328



Internal ID18606548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:84162095..84162595hg38UCSC Ensembl
Innerchr8:85074330..85074830hg19UCSC Ensembl
Innerchr8:85236885..85237385hg18UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2509830, nssv2509836, nssv2509832, nssv2509834, nssv2509837, nssv2509829, nssv2509833, nssv2509828, nssv2509835, nssv2509831
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)nsv971328
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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