A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037578



Internal ID19126797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20401433..21065709hg38UCSC Ensembl
Innerchr15:20606686..21271038hg19UCSC Ensembl
Innerchr15:18866700..19535697hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38664277
hg19664353
hg18668998
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2232n100
Supporting Variantsnssv3540827
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)nsv1037578
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