A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011489



Internal ID19100706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:120601757..120626294hg38UCSC Ensembl
Innerchr4:121522912..121547449hg19UCSC Ensembl
Innerchr4:121742362..121766899hg18UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3824538
hg1924538
hg1824538
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5375n100
Supporting Variantsnssv3639356
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)nsv1011489
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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