A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432119



Internal ID21089672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:132367545..132367957hg38UCSC Ensembl
chr7:132052304..132052716hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg38413
hg19413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150974
Samples
Known GenesPLXNA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432119
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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