A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13684705



Internal ID21206562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15592532..15592643hg38UCSC Ensembl
chr3:15634039..15634150hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2807802
Supporting Variants
Samples
Known GenesHACL1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13684705
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.984375


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