A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18077576



Internal ID20644616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:133905721..133909302hg38UCSC Ensembl
chr2:134663292..134666873hg19UCSC Ensembl
Cytoband2q21.2
Allele length
AssemblyAllele length
hg383582
hg193582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6337351
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18077576
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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