A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193603



Internal ID20760643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:30919401..30983500hg38UCSC Ensembl
chr10:31208330..31272429hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3864100
hg1964100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451374
Supporting Variants
Samples
Known GenesZNF438
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193603
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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