A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972380



Internal ID18607596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63110185..63113756hg38UCSC Ensembl
Innerchr9:67015157..67018728hg19UCSC Ensembl
Innerchr9:66754977..66758548hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg383572
hg193572
hg183572
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2737873, nssv2737872, nssv2737877, nssv2737878, nssv2737881, nssv2737875, nssv2737874, nssv2737880, nssv2737879, nssv2737876
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC286297
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972380
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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