A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5493876



Internal ID271040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:154058295..154059085hg38UCSC Ensembl
chr7:153755380..153756170hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg38791
hg19791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17005915
Samples
Known GenesDPP6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5493876
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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