A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18009665



Internal ID20576705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:51361025..51361748hg38UCSC Ensembl
chr13:51935161..51935884hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38724
hg19724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6484106
Supporting Variants
Samples
Known GenesINTS6, SERPINE3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18009665
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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