A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490827



Internal ID21148380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38321736..38322265hg38UCSC Ensembl
chr13:38895873..38896402hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38530
hg19530
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18008601
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490827
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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