A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5474602



Internal ID252258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28961155..28961420hg38UCSC Ensembl
chr7:29000771..29001036hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16994627
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5474602
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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