A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18007634



Internal ID20574674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:19840801..19842000hg38UCSC Ensembl
chr13:20414941..20416140hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6493769
Supporting Variants
Samples
Known GenesZMYM5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18007634
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00019


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