A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702895



Internal ID126561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64090113..64091223hg38UCSC Ensembl
chr15:64382312..64383422hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381111
hg191111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5530099
Supporting Variants
Samples
Known GenesFAM96A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702895
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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