A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468392



Internal ID21125945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:40984990..41003696hg38UCSC Ensembl
chr11:41006540..41025246hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3818707
hg1918707
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990963
Samples
Known GenesLRRC4C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468392
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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