A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13679675



Internal ID21201533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:203373189..203373247hg38UCSC Ensembl
chr1:203342317..203342375hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2801261
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13679675
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.625


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