A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485657



Internal ID21143210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73381403..73434717hg38UCSC Ensembl
chr13:73955540..74008854hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg3853315
hg1953315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18012567
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485657
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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