A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896324



Internal ID22671415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:68520076..68532497hg38UCSC Ensembl
chr6:69229968..69242389hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3812422
hg1912422
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432358
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896324
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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