A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464069



Internal ID21121622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73528199..73528985hg38UCSC Ensembl
chr11:73239244..73240030hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38787
hg19787
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992831
Samples
Known GenesFAM168A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464069
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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