A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053376



Internal ID19142595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22572335..23089622hg38UCSC Ensembl
Innerchr15:22783446..23300761hg19UCSC Ensembl
Innerchr15:20334810..20852202hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38517288
hg19517316
hg18517393
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2406n100
Supporting Variantsnssv3538878
Samples
Known GenesCYFIP1, GOLGA8I, HERC2P2, LOC283683, NIPA1, NIPA2, TUBGCP5, WHAMMP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053376
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer