A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4016364



Internal ID22077995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41052084..41103534hg38UCSC Ensembl
Outerchr3:41044490..41106066hg38UCSC Ensembl
Innerchr3:41093575..41145025hg19UCSC Ensembl
Outerchr3:41085981..41147557hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3861577
hg1961577
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155961
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4016364
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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