A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899654



Internal ID22674786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151340212..151345354hg38UCSC Ensembl
chr6:151661347..151666489hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg385143
hg195143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412851
Samples
Known GenesAKAP12
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899654
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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