A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023082



Internal ID19112299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:149627686..149753518hg38UCSC Ensembl
Innerchr4:150548838..150674670hg19UCSC Ensembl
Innerchr4:150768288..150894120hg18UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38125833
hg19125833
hg18125833
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3636074
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)nsv1023082
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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