A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926427



Internal ID22701654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23255945..23256109hg38UCSC Ensembl
chr8:23113458..23113622hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430248
Samples
Known GenesCHMP7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926427
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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