A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18009140



Internal ID20576183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44681889..44683625hg38UCSC Ensembl
chr13:45256025..45257761hg19UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg381737
hg191737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6477069
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18009140
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00019


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