A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18089140



Internal ID20656180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:58102161..58102930hg38UCSC Ensembl
chr2:58329296..58330065hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38770
hg19770
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6346528
Supporting Variants
Samples
Known GenesVRK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18089140
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00043


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