A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457112



Internal ID21114665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120390162..120390827hg38UCSC Ensembl
chr11:120260871..120261536hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38666
hg19666
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987257
Samples
Known GenesARHGEF12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457112
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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