A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18081386



Internal ID20648426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:174381395..174382379hg38UCSC Ensembl
chr2:175246123..175247107hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38985
hg19985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6350551
Supporting Variants
Samples
Known GenesCIR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18081386
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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