A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029074



Internal ID19118293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:15520..164078hg38UCSC Ensembl
Innerchr5:15520..164193hg19UCSC Ensembl
Innerchr5:68520..217193hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38148559
hg19148674
hg18148674
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5515n100
Supporting Variantsnssv3744580, nssv3636537, nssv3636538
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)nsv1029074
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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