A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039798



Internal ID18782329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28724126..30158154hg38UCSC Ensembl
Innerchr15:28969272..30450357hg19UCSC Ensembl
Innerchr15:26768313..28237649hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg381434029
hg191481086
hg181469337
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3545674
Samples
Known GenesAPBA2, FAM189A1, GOLGA6L7P, GOLGA8J, GOLGA8T, LOC100289656, LOC646278, NDNL2, TJP1, ULK4P1, ULK4P2, ULK4P3, WHAMMP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039798
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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