A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969645



Internal ID18604872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63014521..63023326hg38UCSC Ensembl
Innerchr9:66919493..66928298hg19UCSC Ensembl
Innerchr9:66659313..66668118hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg388806
hg198806
hg188806
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2738038, nssv2737238, nssv2738039, nssv2738037, nssv2737241, nssv2737240, nssv2737243, nssv2737242, nssv2737239, nssv2738036
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969645
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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