A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178731



Internal ID20745771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:82052201..82542400hg38UCSC Ensembl
chr17:80010077..80500276hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38490200
hg19490200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533522
Supporting Variants
Samples
Known GenesC17orf62, CCDC57, CD7, CSNK1D, DUS1L, FASN, FOXK2, GPS1, HEXDC, MIR6787, NARF, OGFOD3, SECTM1, SLC16A3, TEX19, UTS2R
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178731
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.02698


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