A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887972



Internal ID22662971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:82357737..82359596hg38UCSC Ensembl
chr6:83067454..83069313hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg381860
hg191860
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441927
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887972
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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