A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322084



Internal ID20855193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25381801..25397700hg38UCSC Ensembl
chr1:25708292..25724191hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3815900
hg1915900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv133n223
Supporting Variantsnssv18202837
Samples
Known GenesRHCE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322084
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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