A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18145999



Internal ID20713039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:84796862..84797198hg38UCSC Ensembl
chr6:85506580..85506916hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6414043
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18145999
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00236


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