A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474824



Internal ID21132377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60412001..60413500hg38UCSC Ensembl
chr11:60179474..60180973hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992505
Samples
Known GenesMS4A14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474824
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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