A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18092237



Internal ID20659277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:84909523..84909991hg38UCSC Ensembl
chr2:85136647..85137115hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38469
hg19469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6351305
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18092237
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00366


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