A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188965



Internal ID20756005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38522022..38527053hg38UCSC Ensembl
chr17:36678258..36683288hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg385032
hg195031
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6511288
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188965
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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