A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924058



Internal ID22699285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26208607..26212023hg38UCSC Ensembl
chr7:26248227..26251643hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg383417
hg193417
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446730
Samples
Known GenesCBX3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924058
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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