A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464698



Internal ID21122251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64038707..64039439hg38UCSC Ensembl
chr11:63806179..63806911hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38733
hg19733
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993830
Samples
Known GenesMACROD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464698
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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