A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18079019



Internal ID20646060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:146518401..146519700hg38UCSC Ensembl
chr2:147275969..147277268hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6336736
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18079019
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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