A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047588



Internal ID18790119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:66227169..66394432hg38UCSC Ensembl
Innerchr15:66519507..66686770hg19UCSC Ensembl
Innerchr15:64306561..64473824hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38167264
hg19167264
hg18167264
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3717955
Samples
Known GenesDIS3L, MAP2K1, MEGF11, SCARNA14, TIPIN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047588
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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