A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199889



Internal ID20766929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20703181..20703567hg38UCSC Ensembl
chr1:21029674..21030060hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6326726
Supporting Variants
Samples
Known GenesKIF17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199889
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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