A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18078482



Internal ID20645523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:150972355..151198811hg38UCSC Ensembl
chr2:151828869..152055325hg19UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg38226457
hg19226457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6340417
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18078482
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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