A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042041



Internal ID19131260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20376186..20734174hg38UCSC Ensembl
Innerchr15:20581439..20939503hg19UCSC Ensembl
Innerchr15:18841453..19199516hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38357989
hg19358065
hg18358064
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2233n100
Supporting Variantsnssv3535898
Samples
Known GenesGOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042041
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