A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981896



Internal ID18617092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:60001..63067hg38UCSC Ensembl
Innerchr8:10001..13067hg19UCSC Ensembl
Innerchr8:1..3067hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg383067
hg193067
hg183067
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2721009, nssv2721016, nssv2721012, nssv2721014, nssv2721007, nssv2721015, nssv2721011, nssv2721013, nssv2721008, nssv2721010
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)nsv981896
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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