A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486784



Internal ID21144337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106656699..106657285hg38UCSC Ensembl
chr13:107309047..107309633hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38587
hg19587
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007024
Samples
Known GenesLINC00443
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486784
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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