A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324898



Internal ID20858028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:213052635..213059669hg38UCSC Ensembl
chr1:213225977..213233011hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg387035
hg197035
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200548
Samples
Known GenesRPS6KC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324898
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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