A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465649



Internal ID21123202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126563942..126565635hg38UCSC Ensembl
chr11:126433837..126435530hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg381694
hg191694
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987346
Samples
Known GenesKIRREL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465649
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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