A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2793552



Internal ID21238890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:34506226..34506226hg38UCSC Ensembl
chr13:35080363..35080363hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13680848
Samples
Known GenesLINC00457
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2793552
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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