A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18131851



Internal ID20698891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:62036729..62037069hg38UCSC Ensembl
chr5:61332556..61332896hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6403099
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18131851
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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