A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5543102



Internal ID195939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:154545524..154545548hg38UCSC Ensembl
chr7:154242609..154242633hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17006813
Samples
Known GenesDPP6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5543102
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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