A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971298



Internal ID18606518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:36278065..36279152hg38UCSC Ensembl
Innerchr8:36135583..36136670hg19UCSC Ensembl
Innerchr8:36255125..36256212hg18UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg381088
hg191088
hg181088
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2500096, nssv2500095, nssv2500101, nssv2500103, nssv2500097, nssv2500102, nssv2500098, nssv2500099, nssv2500100, nssv2500104
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv971298
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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