A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18007075



Internal ID20574116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:107110001..107112100hg38UCSC Ensembl
chr13:107762349..107764448hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6487997
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18007075
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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