A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5481744



Internal ID259214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141838001..141838058hg38UCSC Ensembl
chr7:141537801..141537858hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17004463
Samples
Known GenesPRSS37
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5481744
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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