A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5427282



Internal ID206189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9110248..9121058hg38UCSC Ensembl
chr1:9170307..9181117hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3810811
hg1910811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7n206
Supporting Variantsnssv16890089
Samples
Known GenesGPR157
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5427282
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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