A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5492826



Internal ID270024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107183870..107183961hg38UCSC Ensembl
chr7:106824315..106824406hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17000258
Samples
Known GenesHBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5492826
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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