A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042876



Internal ID19132095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20351177..21005431hg38UCSC Ensembl
Innerchr15:20556430..21210760hg19UCSC Ensembl
Innerchr15:18816444..19475419hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38654255
hg19654331
hg18658976
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2232n100
Supporting Variantsnssv3713764
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, NF1P2, POTEB, POTEB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042876
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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