A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029199



Internal ID19118418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:143999409..144037625hg38UCSC Ensembl
Innerchr4:144920562..144958778hg19UCSC Ensembl
Innerchr4:145140012..145178228hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3838217
hg1938217
hg1838217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5429n100
Supporting Variantsnssv3635284
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)nsv1029199
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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