A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909307



Internal ID22684517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:46148534..46148959hg38UCSC Ensembl
chr7:46188132..46188557hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg38426
hg19426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446923
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909307
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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