A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17616877



Internal ID21808924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:48847333..48847429hg38UCSC Ensembl
chr13:49421469..49421565hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6023721
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17616877
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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