A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18138528



Internal ID20705568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:140051008..140051444hg38UCSC Ensembl
chr6:140372145..140372581hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6600950
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18138528
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00057


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