A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2623009



Internal ID17887169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:84173076..84175278hg38UCSC Ensembl
Innerchr14:84639420..84641622hg19UCSC Ensembl
Innerchr14:83709173..83711375hg18UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg382203
hg192203
hg182203
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv976772
Supporting Variants
SamplesHGDP01307
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Hsa
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2623009
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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