A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18009807



Internal ID20576847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:45712901..45714500hg38UCSC Ensembl
chr13:46287036..46288635hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6491701
Supporting Variants
Samples
Known GenesSPERT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18009807
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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