A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18077932



Internal ID20644973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:13631866..13632634hg38UCSC Ensembl
chr2:13771991..13772759hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38769
hg19769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6353088
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18077932
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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