A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2737648



Internal ID17795700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62478388..62483055hg38UCSC Ensembl
Innerchr9:46789689..46794356hg19UCSC Ensembl
Innerchr9:46629685..46634352hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg384668
hg194668
hg184668
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv973296
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)nssv2737648
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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