A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401566



Internal ID21059119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:53972714..53973013hg38UCSC Ensembl
chr5:53268544..53268843hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132413
Samples
Known GenesARL15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401566
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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