A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16985369



Internal ID57654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89596808..89600759hg38UCSC Ensembl
chr6:90306527..90310478hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg383952
hg193952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5465795
Supporting Variants
Samples
Known GenesANKRD6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16985369
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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