A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034223



Internal ID19123445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:4030474..4060113hg38UCSC Ensembl
Innerchr6:4030708..4060347hg19UCSC Ensembl
Innerchr6:3975707..4005346hg18UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3829640
hg1929640
hg1829640
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654726
Samples
Known GenesPRPF4B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034223
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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