A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029420



Internal ID19118639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:130605780..130712011hg38UCSC Ensembl
Innerchr4:131526935..131633166hg19UCSC Ensembl
Innerchr4:131746385..131852616hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38106232
hg19106232
hg18106232
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3743099, nssv3639452, nssv3639450, nssv3639451
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029420
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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