A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18009664



Internal ID20576704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:51358491..51358922hg38UCSC Ensembl
chr13:51932627..51933058hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38432
hg19432
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6487734
Supporting Variants
Samples
Known GenesSERPINE3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18009664
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00042


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