A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488686



Internal ID21146239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26449774..26474209hg38UCSC Ensembl
chr13:27023911..27048346hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3824436
hg1924436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007459
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488686
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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