A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468078



Internal ID21125631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78476401..78478800hg38UCSC Ensembl
chr11:78187447..78189846hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994199
Samples
Known GenesNARS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468078
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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