A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052565



Internal ID20619605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:163192051..163192610hg38UCSC Ensembl
chr1:163161841..163162400hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318935
Supporting Variants
Samples
Known GenesRGS5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052565
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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