A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973228



Internal ID18608443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42259956..42267528hg38UCSC Ensembl
Innerchr9:41243574..41251149hg19UCSC Ensembl
Innerchr9:41233574..41241149hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg387573
hg197576
hg187576
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2727262, nssv2727263, nssv2727257, nssv2727261, nssv2727259, nssv2727256, nssv2727265, nssv2727258, nssv2727264, nssv2727260
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)nsv973228
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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