A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18008933



Internal ID20575975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:41090517..41115042hg38UCSC Ensembl
chr13:41664653..41689178hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3824526
hg1924526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6484422
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18008933
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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