A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2764512



Internal ID17799304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:111191695..111194726hg38UCSC Ensembl
Innerchr3:110910542..110913573hg19UCSC Ensembl
Innerchr3:112393232..112396263hg18UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg383032
hg193032
hg183032
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv963553
Supporting Variants
SamplesHGDP00778
Known GenesPVRL3
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2764512
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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