A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556328



Internal ID329467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:154541662..154543934hg38UCSC Ensembl
chr7:154238747..154241019hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg382273
hg192273
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17006810
Samples
Known GenesDPP6
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556328
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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