A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18015501



Internal ID20582541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96915880..96916296hg38UCSC Ensembl
chr13:97568134..97568550hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38417
hg19417
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6485102
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18015501
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00284


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