A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902320



Internal ID22677477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:143105285..143110241hg38UCSC Ensembl
chr6:143426422..143431378hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg384957
hg194957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427921
Samples
Known GenesAIG1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902320
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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