A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5477579



Internal ID255154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128469325..128472180hg38UCSC Ensembl
chr7:128109379..128112234hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg382856
hg192856
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17005172
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5477579
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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