A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027434



Internal ID19116653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:155139619..155156105hg38UCSC Ensembl
Innerchr4:156060771..156077257hg19UCSC Ensembl
Innerchr4:156280221..156296707hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3816487
hg1916487
hg1816487
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3636132
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)nsv1027434
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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