A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921270



Internal ID22696493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:105533825..105533937hg38UCSC Ensembl
chr8:106546053..106546165hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444004
Samples
Known GenesZFPM2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921270
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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