A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13688469



Internal ID21210325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:44239970..44241693hg38UCSC Ensembl
chr2:44467109..44468832hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg381724
hg191724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2807500
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13688469
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.125


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