A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2742702



Internal ID17873975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:67914326..67919820hg38UCSC Ensembl
Innerchr9:67981772..67987266hg19UCSC Ensembl
Innerchr9:67571592..67577086hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg385495
hg195495
hg185495
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv982498
Supporting Variants
SamplesHGDP01284
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2742702
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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