A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868480



Internal ID22643415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:77570407..77570560hg38UCSC Ensembl
chr1:78036092..78036245hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17380847
Samples
Known GenesZZZ3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868480
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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