A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972795



Internal ID18608011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:101501331..101501831hg38UCSC Ensembl
Innerchr9:104263613..104264113hg19UCSC Ensembl
Innerchr9:103303434..103303934hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2564445, nssv2564447, nssv2564448, nssv2564441, nssv2564442, nssv2564444, nssv2564440, nssv2564439, nssv2564446, nssv2564443
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)nsv972795
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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