A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982970



Internal ID18618164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:2329864..2335606hg38UCSC Ensembl
Innerchr11:2351094..2356836hg19UCSC Ensembl
Innerchr11:2307670..2313412hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg385743
hg195743
hg185743
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1871651, nssv1871654, nssv1871652, nssv1871650, nssv1871649, nssv1871655, nssv1871658, nssv1871657, nssv1871653, nssv1871656
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCD81-AS1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982970
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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