A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494890



Internal ID21152443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:71968523..71969186hg38UCSC Ensembl
chr13:72542661..72543324hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38664
hg19664
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18012716
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494890
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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