A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903016



Internal ID22678180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108930846..108932778hg38UCSC Ensembl
chr6:109252049..109253981hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381933
hg191933
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426309
Samples
Known GenesARMC2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903016
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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