A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16983921



Internal ID56661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:79802641..79808352hg38UCSC Ensembl
chr6:80512358..80518069hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg385712
hg195712
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5460172
Supporting Variants
Samples
Known GenesC6orf7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16983921
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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