A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181908



Internal ID20748948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81809211..81809586hg38UCSC Ensembl
chr17:79767087..79767462hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38376
hg19376
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528369
Supporting Variants
Samples
Known GenesGCGR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181908
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00074


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