A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032139



Internal ID19121361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:15520..179011hg38UCSC Ensembl
Innerchr5:15520..179126hg19UCSC Ensembl
Innerchr5:68520..232126hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38163492
hg19163607
hg18163607
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5515n100
Supporting Variantsnssv3636541
Samples
Known GenesPLEKHG4B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032139
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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