A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915051



Internal ID22690269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:132404161..132404863hg38UCSC Ensembl
chr7:132088920..132089622hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg38703
hg19703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17433579
Samples
Known GenesPLXNA4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915051
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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