A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011674



Internal ID19100891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:11154521..11203057hg38UCSC Ensembl
Innerchr4:11156145..11204681hg19UCSC Ensembl
Innerchr4:10765243..10813779hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3848537
hg1948537
hg1848537
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3619755
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)nsv1011674
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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