A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467242



Internal ID21124795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60093427..60115827hg38UCSC Ensembl
chr11:59860900..59883300hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3822401
hg1922401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992482
Samples
Known GenesMS4A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467242
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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