A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189773



Internal ID20756813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:2850246..2926216hg38UCSC Ensembl
chr17:2753540..2829510hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3875971
hg1975971
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498837
Supporting Variants
Samples
Known GenesRAP1GAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189773
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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