A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475896



Internal ID21133449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32011684..32027973hg38UCSC Ensembl
chr13:32585821..32602110hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg3816290
hg1916290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18008583
Samples
Known GenesFRY-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475896
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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