A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189411



Internal ID20756451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64205689..64333408hg38UCSC Ensembl
chr17:62283049..62410760hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38127720
hg19127712
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6520482
Supporting Variants
Samples
Known GenesPECAM1, TEX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189411
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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