A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484049



Internal ID21141602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87295374..87444401hg38UCSC Ensembl
chr13:87947629..88096656hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38149028
hg19149028
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18013859
Samples
Known GenesMIR4500HG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484049
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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