A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561351



Internal ID334334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:122831645..122833085hg38UCSC Ensembl
chr7:122471699..122473139hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg381441
hg191441
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17003432
Samples
Known GenesCADPS2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561351
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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