A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16990685



Internal ID61204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169475195..169486072hg38UCSC Ensembl
chr6:169875290..169886167hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3810878
hg1910878
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5460179
Supporting Variants
Samples
Known GenesWDR27
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16990685
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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