A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17616281



Internal ID21808328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:40833483..40840911hg38UCSC Ensembl
chr13:41407619..41415047hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg387429
hg197429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6026015
Supporting Variants
Samples
Known GenesTPTE2P5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17616281
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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