A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090436



Internal ID21267569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:6729431..6766347hg38UCSC Ensembl
Innerchr1:6789491..6826407hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg3836917
hg1936917
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113982
Supporting Variants
Samplessample113
Known GenesLOC100505887
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090436
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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