A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922688



Internal ID22697913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166925011..166925171hg38UCSC Ensembl
chr6:167338499..167338659hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424955
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922688
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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