A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900605



Internal ID22675748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28372991..28385246hg38UCSC Ensembl
chr6:28340768..28353023hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3812256
hg1912256
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17449050
Samples
Known GenesZSCAN12
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900605
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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