A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7n206



Internal ID22755311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9109345..9121058hg38UCSC Ensembl
chr1:9169404..9181117hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3811714
hg1911714
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5427282, nsv5415738
Samples
Known GenesGPR157
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv7n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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