A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925291



Internal ID22700518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:78699918..78700513hg38UCSC Ensembl
chr8:79612153..79612748hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg38596
hg19596
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437119
Samples
Known GenesZC2HC1A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925291
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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