A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963551



Internal ID18598792
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2766623
SamplesHGDP01284
Known GenesTBC1D5
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963551
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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