A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18085855



Internal ID20652895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:21771691..21772312hg38UCSC Ensembl
chr2:21994563..21995184hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38622
hg19622
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6340252
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18085855
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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