A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908228



Internal ID22683438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149233920..149234080hg38UCSC Ensembl
chr7:148931011..148931171hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445514
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908228
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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