A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18008842



Internal ID20575884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:34490001..34494500hg38UCSC Ensembl
chr13:35064138..35068637hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg384500
hg194500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6486088
Supporting Variants
Samples
Known GenesLINC00457
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18008842
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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