A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754436



Internal ID20530296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:203839997..203839997hg38UCSC Ensembl
chr1:203809125..203809125hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38703
hg19703
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288480
Samples
Known GenesZC3H11A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754436
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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