A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919395



Internal ID22694617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:144784494..144784627hg38UCSC Ensembl
chr8:146009879..146010012hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439618
Samples
Known GenesZNF34
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919395
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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