A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17699788



Internal ID123454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42507887..42508564hg38UCSC Ensembl
chr15:42800085..42800762hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38678
hg19678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497086
Supporting Variants
Samples
Known GenesSNAP23
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17699788
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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