A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2809521



Internal ID21254859
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 StatusM
Merged Variants
Supporting Variantsnssv13703383
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2809521
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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