A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920599



Internal ID22695822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:113923111..113923163hg38UCSC Ensembl
chr7:113563166..113563218hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432364
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920599
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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