A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610432



Internal ID20983503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24871932..24872531hg38UCSC Ensembl
chr7:24911551..24912150hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226282
Samples
Known GenesOSBPL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610432
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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