A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13695577



Internal ID21217428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112282693..112282831hg38UCSC Ensembl
chr13:112937007..112937145hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2793059
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13695577
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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