A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18138683



Internal ID20705723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:125606885..125609155hg38UCSC Ensembl
chr6:125928031..125930301hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg382271
hg192271
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6618142
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18138683
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01571


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