A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016311



Internal ID19105530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:171484847..171581059hg38UCSC Ensembl
Innerchr4:172405998..172502210hg19UCSC Ensembl
Innerchr4:172642573..172738785hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3896213
hg1996213
hg1896213
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5475n100
Supporting Variantsnssv3635432
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)nsv1016311
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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