A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5958734



Internal ID22733796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123260608..123260608hg38UCSC Ensembl
chr8:124272848..124272848hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444420
Samples
Known GenesZHX1, ZHX1-C8ORF76
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5958734
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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