A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385722



Internal ID21043275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:225016..406153hg38UCSC Ensembl
chr5:225131..406268hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38181138
hg19181138
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215680
Samples
Known GenesAHRR, LOC102467073, PDCD6, SDHA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385722
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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