A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484315



Internal ID21141868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110556851..110558877hg38UCSC Ensembl
chr13:111209198..111211224hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg382027
hg192027
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007153
Samples
Known GenesRAB20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484315
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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