A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18007496



Internal ID20574536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27263406..27268843hg38UCSC Ensembl
chr13:27837543..27842980hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg385438
hg195438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6488521
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18007496
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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