A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433027



Internal ID21395029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206551673..206584668hg38UCSC Ensembl
chr1:206725001..206758000hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3832996
hg1933000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15751497
SamplesSMI041
Known GenesRASSF5
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433027
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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