A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18126345



Internal ID20693385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:119279961..119280573hg38UCSC Ensembl
chr5:118615656..118616268hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38613
hg19613
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6414291
Supporting Variants
Samples
Known GenesTNFAIP8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18126345
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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