A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900467



Internal ID22675610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:114164699..114517903hg38UCSC Ensembl
chr6:114485863..114839067hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38353205
hg19353205
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419021
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900467
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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