A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18135491



Internal ID20702531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112735301..112736200hg38UCSC Ensembl
chr6:113056503..113057402hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6603153
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18135491
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.003


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