A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327440



Internal ID20860579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:241738001..241929400hg38UCSC Ensembl
chr1:241901303..242092702hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38191400
hg19191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059094
Samples
Known GenesEXO1, WDR64
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327440
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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