A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021372



Internal ID19110589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:176387516..176438246hg38UCSC Ensembl
Innerchr4:177308667..177359397hg19UCSC Ensembl
Innerchr4:177545661..177596391hg18UCSC Ensembl
Cytoband4q34.2
Allele length
AssemblyAllele length
hg3850731
hg1950731
hg1850731
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5480n100
Supporting Variantsnssv3635459
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)nsv1021372
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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