A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486761



Internal ID21144314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:43921526..43932008hg38UCSC Ensembl
chr13:44495662..44506144hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3810483
hg1910483
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18009100
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486761
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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