A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484581



Internal ID21142134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:21343303..21361874hg38UCSC Ensembl
chr13:21917442..21936013hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3818572
hg1918572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007998
Samples
Known GenesLINC00539, MIPEPP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484581
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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