A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704238



Internal ID127904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64815341..64837137hg38UCSC Ensembl
chr15:65107540..65129336hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3821797
hg1921797
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5526353
Supporting Variants
Samples
Known GenesPIF1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704238
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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