A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18033317



Internal ID20600357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:13906583..13911056hg38UCSC Ensembl
chr17:13809900..13814373hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg384474
hg194474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6509054
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18033317
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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