A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473474



Internal ID21131027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126599431..126604641hg38UCSC Ensembl
chr11:126469326..126474536hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg385211
hg195211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987351
Samples
Known GenesKIRREL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473474
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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