A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18077559



Internal ID20644599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:133683365..133686327hg38UCSC Ensembl
chr2:134440936..134443898hg19UCSC Ensembl
Cytoband2q21.2
Allele length
AssemblyAllele length
hg382963
hg192963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6341446
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18077559
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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