A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909213



Internal ID22684423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:47076252..47093599hg38UCSC Ensembl
chr7:47115850..47133197hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3817348
hg1917348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440236
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909213
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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