A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16990692



Internal ID61210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169551564..169552065hg38UCSC Ensembl
chr6:169951660..169952161hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457042
Supporting Variants
Samples
Known GenesWDR27
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16990692
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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