A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17617359



Internal ID21809406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39893736..39893789hg38UCSC Ensembl
chr15:40185937..40185990hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6035725
Supporting Variants
Samples
Known GenesGPR176
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17617359
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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