A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019534



Internal ID19108752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:176387516..176427206hg38UCSC Ensembl
Innerchr4:177308667..177348357hg19UCSC Ensembl
Innerchr4:177545661..177585351hg18UCSC Ensembl
Cytoband4q34.2
Allele length
AssemblyAllele length
hg3839691
hg1939691
hg1839691
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5480n100
Supporting Variantsnssv3744524
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)nsv1019534
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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