A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18057610



Internal ID20624650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21756031..21756353hg38UCSC Ensembl
chr1:22082524..22082846hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331328
Supporting Variants
Samples
Known GenesUSP48
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18057610
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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