A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184933



Internal ID20751973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:40682883..40699164hg38UCSC Ensembl
chr17:38839135..38855416hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3816282
hg1916282
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514015
Supporting Variants
Samples
Known GenesKRT24
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184933
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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