A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024138



Internal ID19113355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:143955508..144080924hg38UCSC Ensembl
Innerchr4:144876661..145002077hg19UCSC Ensembl
Innerchr4:145096111..145221527hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38125417
hg19125417
hg18125417
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635237
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)nsv1024138
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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