A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908594



Internal ID22683804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90336050..90338119hg38UCSC Ensembl
chr7:89965364..89967433hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg382070
hg192070
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437399
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908594
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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