A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485439



Internal ID21142992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96855477..96915499hg38UCSC Ensembl
chr13:97507731..97567753hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3860023
hg1960023
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18015497
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485439
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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