A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982464



Internal ID18270973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39150110..39150914hg38UCSC Ensembl
Innerchr9:65584759..65585559hg19UCSC Ensembl
Innerchr9:65324579..65325379hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38805
hg19801
hg18801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2738637, nssv2738634, nssv2738630, nssv2738631, nssv2738633, nssv2738639, nssv2738636, nssv2738638, nssv2738632, nssv2738635
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)nsv982464
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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