A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461564



Internal ID21119117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:40796936..40921176hg38UCSC Ensembl
chr11:40818486..40942726hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38124241
hg19124241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990934
Samples
Known GenesLRRC4C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461564
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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