A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14092112



Internal ID21274780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:144000430..144115603hg38UCSC Ensembl
Innerchr4:144921583..145036756hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38115174
hg19115174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112016
Supporting Variants
Samplessample211
Known GenesGYPA, GYPB
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14092112
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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