A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030755



Internal ID19119974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:156046811..156069699hg38UCSC Ensembl
Innerchr4:156967963..156990851hg19UCSC Ensembl
Innerchr4:157187413..157210301hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3822889
hg1922889
hg1822889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5444n100
Supporting Variantsnssv3636140
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)nsv1030755
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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