A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973254



Internal ID18608469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65217309..65219924hg38UCSC Ensembl
Innerchr9:42782677..42785294hg19UCSC Ensembl
Innerchr9:42772673..42775290hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg382616
hg192618
hg182618
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2731256, nssv2731260, nssv2731261, nssv2731262, nssv2731259, nssv2731258, nssv2731264, nssv2731255, nssv2731257, nssv2731263
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)nsv973254
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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