A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16982609



Internal ID55769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:53765523..53799174hg38UCSC Ensembl
chr6:53630321..53663972hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3833652
hg1933652
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5456060
Supporting Variants
Samples
Known GenesLRRC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16982609
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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