A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914876



Internal ID22690093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26201826..26206365hg38UCSC Ensembl
chr7:26241446..26245985hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg384540
hg194540
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444394
Samples
Known GenesCBX3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914876
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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