A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5476496



Internal ID254104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106287297..106304923hg38UCSC Ensembl
chr7:105927743..105945369hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3817627
hg1917627
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17000900
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5476496
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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