A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13682947



Internal ID21204804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150821840..150821973hg38UCSC Ensembl
chr3:150539627..150539760hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2806833
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13682947
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency1


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