A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029304



Internal ID19118523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:143995988..144090345hg38UCSC Ensembl
Innerchr4:144917141..145011498hg19UCSC Ensembl
Innerchr4:145136591..145230948hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3894358
hg1994358
hg1894358
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5428n100
Supporting Variantsnssv3635253
Samples
Known GenesGYPB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029304
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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