A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433109



Internal ID21395111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27036347..27037321hg38UCSC Ensembl
chr1:27362838..27363812hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38975
hg19975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15746772
SamplesSMI018
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433109
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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