A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923675



Internal ID22698902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166898838..166898895hg38UCSC Ensembl
chr6:167312326..167312383hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419327
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923675
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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