A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2737886



Internal ID17799998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63143012..63148806hg38UCSC Ensembl
Innerchr9:67047984..67053778hg19UCSC Ensembl
Innerchr9:66787804..66793598hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg385795
hg195795
hg185795
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv973686
Supporting Variants
SamplesHGDP00778
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2737886
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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