A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18079938



Internal ID20646978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:168903397..168903964hg38UCSC Ensembl
chr2:169759907..169760474hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38568
hg19568
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6341302
Supporting Variants
Samples
Known GenesG6PC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18079938
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00029


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