A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5476283



Internal ID253896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26515328..26515708hg38UCSC Ensembl
chr7:26554947..26555327hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38381
hg19381
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16994974
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5476283
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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