A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475900



Internal ID21133453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:57562120..58247494hg38UCSC Ensembl
chr13:58136254..58821628hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38685375
hg19685375
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178800
Samples
Known GenesPCDH17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475900
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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