A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112016



Internal ID21295282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:144000430..144115603hg38UCSC Ensembl
Innerchr4:144921583..145036756hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38115174
hg19115174
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14092112, nssv14093398, nssv14094904, nssv14090517
Samplessample282, sample156, sample211, sample391
Known GenesGYPA, GYPB
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112016
Frequency
Sample Size467
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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