A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469135



Internal ID21126688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120678362..120683058hg38UCSC Ensembl
chr11:120549071..120553767hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg384697
hg194697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987276
Samples
Known GenesGRIK4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469135
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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