A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18078342



Internal ID20645382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:145647490..145648242hg38UCSC Ensembl
chr2:146405058..146405810hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg38753
hg19753
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6336714
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18078342
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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