A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2792680



Internal ID21238018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:34541261..34541310hg38UCSC Ensembl
chr13:35115398..35115447hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13686916
Samples
Known GenesLINC00457
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2792680
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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