A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1871657



Internal ID17779584
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 Flag1
Merged StatusS
Merged Variantsnsv982970
Supporting Variants
SamplesHGDP00665
Known GenesCD81-AS1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv1871657
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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