A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323822



Internal ID20856944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153612333..153627695hg38UCSC Ensembl
chr1:153584809..153600171hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3815363
hg1915363
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200475
Samples
Known GenesS100A13, S100A14, S100A16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323822
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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