A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972762



Internal ID18607978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:80563690..80566362hg38UCSC Ensembl
Innerchr9:83178605..83181277hg19UCSC Ensembl
Innerchr9:82368425..82371097hg18UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg382673
hg192673
hg182673
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2553696, nssv2553690, nssv2553691, nssv2553693, nssv2553695, nssv2553697, nssv2553688, nssv2553689, nssv2553694, nssv2553692
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)nsv972762
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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