A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469132



Internal ID21126685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62663536..62664064hg38UCSC Ensembl
chr11:62431008..62431536hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38529
hg19529
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993221
Samples
Known GenesC11orf48, LOC102288414
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469132
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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