A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900842



Internal ID22675989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25077145..25172097hg38UCSC Ensembl
chr6:25077373..25172325hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3894953
hg1994953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444777
Samples
Known GenesCMAHP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900842
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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