A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981906



Internal ID18617102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7667128..7774629hg38UCSC Ensembl
Innerchr8:7524650..7632151hg19UCSC Ensembl
Innerchr8:7561977..7669561hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38107502
hg19107502
hg18107585
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2494262, nssv2494258, nssv2494264, nssv2494256, nssv2494260, nssv2494259, nssv2494261, nssv2494265, nssv2494263, nssv2494257
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFAM90A10P
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981906
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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