A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068729



Internal ID20635769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:15788799..15789332hg38UCSC Ensembl
chr21:17161118..17161651hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38534
hg19534
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547113
Supporting Variants
Samples
Known GenesUSP25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068729
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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