A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2766319



Internal ID17508257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:70813066..70829853hg38UCSC Ensembl
Innerchr2:71040198..71056984hg19UCSC Ensembl
Innerchr2:70893706..70910492hg18UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg3816788
hg1916787
hg1816787
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv961756
Supporting Variants
SamplesHGDP01029
Known GenesCLEC4F
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2766319
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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