A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18007516



Internal ID20574556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27766734..27784484hg38UCSC Ensembl
chr13:28340871..28358621hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg3817751
hg1917751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6480128
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18007516
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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