A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489572



Internal ID21147125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:52105984..52121407hg38UCSC Ensembl
chr13:52680120..52695543hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3815424
hg1915424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18009703
Samples
Known GenesNEK5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489572
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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