A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195841



Internal ID20762881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:53743401..53791000hg38UCSC Ensembl
chr17:51820762..51868361hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3847600
hg1947600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6523734
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195841
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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