A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322850



Internal ID20855965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36441477..36441956hg38UCSC Ensembl
chr1:36907078..36907557hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38480
hg19480
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202447
Samples
Known GenesOSCP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322850
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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