A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13703383



Internal ID21225195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:81858343..81858662hg38UCSC Ensembl
chr3:81907494..81907813hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2809521
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13703383
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency1


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