A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014042



Internal ID19103262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68734135..68802278hg38UCSC Ensembl
Innerchr4:69599853..69667996hg19UCSC Ensembl
Innerchr4:69634442..69702585hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3868144
hg1968144
hg1868144
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5290n100
Supporting Variantsnssv3630228
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)nsv1014042
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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