A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16985544



Internal ID57770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96132261..96132359hg38UCSC Ensembl
chr6:96580137..96580235hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5473201
Supporting Variants
Samples
Known GenesFUT9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16985544
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.154855


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