A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006167



Internal ID19095385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:10782262..11060573hg38UCSC Ensembl
Innerchr4:10783886..11062197hg19UCSC Ensembl
Innerchr4:10392984..10671295hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38278312
hg19278312
hg18278312
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3619749
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)nsv1006167
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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