A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910913



Internal ID22686125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:475594..475815hg38UCSC Ensembl
chr7:515231..515452hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444350
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910913
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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