A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18078738



Internal ID20645778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:147423701..147493400hg38UCSC Ensembl
chr2:148181269..148250968hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3869700
hg1969700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6344050
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18078738
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00082


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