A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033921



Internal ID19123143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:143834417..144003772hg38UCSC Ensembl
Innerchr4:144755570..144924925hg19UCSC Ensembl
Innerchr4:144975020..145144375hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38169356
hg19169356
hg18169356
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5416n100
Supporting Variantsnssv3635048
Samples
Known GenesGYPB, GYPE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033921
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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