A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030473



Internal ID19119692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:135967555..136041062hg38UCSC Ensembl
Innerchr4:136888710..136962217hg19UCSC Ensembl
Innerchr4:137108160..137181667hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3873508
hg1973508
hg1873508
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3641113
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)nsv1030473
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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