A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18122099



Internal ID20689139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:102542385..102543008hg38UCSC Ensembl
chr5:101878089..101878712hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38624
hg19624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6399713
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18122099
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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