A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973632



Internal ID18608847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42875158..42880385hg38UCSC Ensembl
Innerchr9:44090734..44095961hg19UCSC Ensembl
Innerchr9:44030730..44035957hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg385228
hg195228
hg185228
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2735548, nssv2735547, nssv2735554, nssv2735551, nssv2735546, nssv2735555, nssv2735553, nssv2735549, nssv2735552, nssv2735550
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)nsv973632
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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