A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18034680



Internal ID20601720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29217759..29221423hg38UCSC Ensembl
chr17:27544777..27548441hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg383665
hg193665
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6509255
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18034680
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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