A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18084964



Internal ID20652004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:203863422..203867009hg38UCSC Ensembl
chr2:204728145..204731732hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg383588
hg193588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6349907
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18084964
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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