A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2793555



Internal ID21238893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:34984495..34990736hg38UCSC Ensembl
chr13:35558632..35564873hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg386242
hg196242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13693504
Samples
Known GenesNBEA
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2793555
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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