A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18131529



Internal ID20698569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:40943028..40982314hg38UCSC Ensembl
chr5:40943130..40982416hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3839287
hg1939287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6385635
Supporting Variants
Samples
Known GenesC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18131529
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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