A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5477257



Internal ID254846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32571435..32572128hg38UCSC Ensembl
chr7:32611047..32611740hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38694
hg19694
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16994404
Samples
Known GenesAVL9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5477257
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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