A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474560



Internal ID21132113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78056829..78059788hg38UCSC Ensembl
chr11:77767875..77770834hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg382960
hg192960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994174
Samples
Known GenesNDUFC2-KCTD14, RNU6-83P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474560
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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