A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2765705



Internal ID17835342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:100634902..100661964hg38UCSC Ensembl
Innerchr14:101101239..101128301hg19UCSC Ensembl
Innerchr14:100170992..100198054hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3827063
hg1927063
hg1827063
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv974480
Supporting Variants
SamplesHGDP00998
Known GenesLINC00523
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2765705
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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