A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110383



Internal ID21293649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:178144882..178159354hg38UCSC Ensembl
Innerchr1:178114017..178128489hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3814473
hg1914473
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14100598
Samplessample395
Known GenesRASAL2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110383
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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