A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18012949



Internal ID20579989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77788971..77789627hg38UCSC Ensembl
chr13:78363106..78363762hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg38657
hg19657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6480718
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18012949
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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