A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178956



Internal ID20745996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44947230..44948137hg38UCSC Ensembl
chr13:45521365..45522272hg19UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg38908
hg19908
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6489323
Supporting Variants
Samples
Known GenesNUFIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178956
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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