A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701599



Internal ID125265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39894914..39895013hg38UCSC Ensembl
chr15:40187115..40187214hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5513697
Supporting Variants
Samples
Known GenesGPR176
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701599
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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