A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457031



Internal ID21114584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65796928..65799930hg38UCSC Ensembl
chr11:65564399..65567401hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg383003
hg193003
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992518
Samples
Known GenesOVOL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457031
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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