A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17699830



Internal ID123496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55958482..55980518hg38UCSC Ensembl
chr15:56250680..56272716hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3822037
hg1922037
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5531497
Supporting Variants
Samples
Known GenesNEDD4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17699830
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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