A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982485



Internal ID18617680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63058397..63065731hg38UCSC Ensembl
Innerchr9:66963369..66970703hg19UCSC Ensembl
Innerchr9:66703189..66710523hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg387335
hg197335
hg187335
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2736935, nssv2736937, nssv2736939, nssv2736934, nssv2736932, nssv2736938, nssv2736936, nssv2736931, nssv2736933, nssv2736930
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)nsv982485
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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