A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18008362



Internal ID20575402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28596089..28596788hg38UCSC Ensembl
chr13:29170226..29170925hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6483012
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18008362
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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