A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18014969



Internal ID20582009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:88159152..88161526hg38UCSC Ensembl
chr13:88811407..88813781hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg382375
hg192375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6479917
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18014969
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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