A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2737625



Internal ID17840818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62425996..62436303hg38UCSC Ensembl
Innerchr9:46737297..46747604hg19UCSC Ensembl
Innerchr9:46577293..46587600hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3810308
hg1910308
hg1810308
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv973295
Supporting Variants
SamplesHGDP00998
Known GenesKGFLP1
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2737625
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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