A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114699



Internal ID21297965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:241794986..241797300hg38UCSC Ensembl
Innerchr1:241958288..241960602hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg382315
hg192315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14093593
Samplessample127
Known GenesWDR64
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114699
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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