A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892086



Internal ID22667131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:68334586..68334871hg38UCSC Ensembl
chr6:69044478..69044763hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38286
hg19286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17434980
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892086
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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