A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180300



Internal ID20747340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32051201..32058400hg38UCSC Ensembl
chr10:32340129..32347328hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg387200
hg197200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437004
Supporting Variants
Samples
Known GenesKIF5B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180300
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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