A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18089227



Internal ID20656267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:63291238..63312984hg38UCSC Ensembl
chr2:63518373..63540119hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg3821747
hg1921747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6341950
Supporting Variants
Samples
Known GenesWDPCP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18089227
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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