A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926078



Internal ID22701305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166901084..166902122hg38UCSC Ensembl
chr6:167314572..167315610hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381039
hg191039
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412576
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926078
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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