A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027468



Internal ID19116687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:138862859..138909900hg38UCSC Ensembl
Innerchr4:139784013..139831054hg19UCSC Ensembl
Innerchr4:140003463..140050504hg18UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3847042
hg1947042
hg1847042
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3641180
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)nsv1027468
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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