A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2766623



Internal ID17864111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:17678194..17682853hg38UCSC Ensembl
Innerchr3:17719686..17724345hg19UCSC Ensembl
Innerchr3:17694690..17699349hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg384660
hg194660
hg184660
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv963551
Supporting Variants
SamplesHGDP01284
Known GenesTBC1D5
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2766623
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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