A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014533



Internal ID19103751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:15179551..15221081hg38UCSC Ensembl
Innerchr4:15181175..15222705hg19UCSC Ensembl
Innerchr4:14790273..14831803hg18UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3841531
hg1941531
hg1841531
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3619842
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)nsv1014533
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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