A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324203



Internal ID20857328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:51709401..51734900hg38UCSC Ensembl
chr1:52175073..52200572hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3825500
hg1925500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201444
Samples
Known GenesOSBPL9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324203
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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