A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433000



Internal ID21395002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:184111846..184112573hg38UCSC Ensembl
chr1:184080980..184081707hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38728
hg19728
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15749101
SamplesNB12
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433000
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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