A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465536



Internal ID21123089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78138866..78139775hg38UCSC Ensembl
chr11:77849912..77850821hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38910
hg19910
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994180
Samples
Known GenesALG8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465536
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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