A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18008566



Internal ID20575607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31675350..31773458hg38UCSC Ensembl
chr13:32249487..32347595hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg3898109
hg1998109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6482963
Supporting Variants
Samples
Known GenesRXFP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18008566
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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