A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461481



Internal ID21119034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:40328675..40329992hg38UCSC Ensembl
chr11:40350225..40351542hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg381318
hg191318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991079
Samples
Known GenesLRRC4C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461481
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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