A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474567



Internal ID21132120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78117328..78128241hg38UCSC Ensembl
chr11:77828374..77839287hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3810914
hg1910914
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994178
Samples
Known GenesALG8, RNU6-83P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474567
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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