A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18083461



Internal ID20650501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:21505116..21505881hg38UCSC Ensembl
chr2:21727988..21728753hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38766
hg19766
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6341884
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18083461
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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