A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2792169



Internal ID21237507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110677266..110677341hg38UCSC Ensembl
chr13:111329613..111329688hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13684398
Samples
Known GenesCARS2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2792169
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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