A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18145972



Internal ID20713012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:84372597..84373292hg38UCSC Ensembl
chr6:85082315..85083010hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38696
hg19696
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6412762
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18145972
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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