A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900809



Internal ID22675955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:143215043..143216154hg38UCSC Ensembl
chr6:143536180..143537291hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg381112
hg191112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414206
Samples
Known GenesAIG1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900809
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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