A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484777



Internal ID262183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:30745893..30746499hg38UCSC Ensembl
chr7:30785509..30786115hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38607
hg19607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16994002
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484777
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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