A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398612



Internal ID21056165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24294158..24435691hg38UCSC Ensembl
chr6:24294386..24435919hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38141534
hg19141534
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217269
Samples
Known GenesDCDC2, GPLD1, KAAG1, MRS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398612
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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