A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13703907



Internal ID21225715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:45377936..45378000hg38UCSC Ensembl
chr13:45952071..45952135hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2792699
Supporting Variants
Samples
Known GenesTPT1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13703907
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.984375


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