A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188997



Internal ID20756037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:70795947..70818447hg38UCSC Ensembl
chr17:68792088..68814588hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3822501
hg1922501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6527668
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188997
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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