A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874098



Internal ID22649048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:203803149..203803259hg38UCSC Ensembl
chr1:203772277..203772387hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359554
Samples
Known GenesZC3H11A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874098
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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