A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219634



Internal ID20786674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:81002396..81176391hg38UCSC Ensembl
chr6:81712113..81886108hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38173996
hg19173996
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6412237
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219634
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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