A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035720



Internal ID18778251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32179274..32565269hg38UCSC Ensembl
Innerchr15:32471475..32857470hg19UCSC Ensembl
Innerchr15:30258767..30644762hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38385996
hg19385996
hg18385996
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2538n100
Supporting Variantsnssv3547786
Samples
Known GenesGOLGA8K, GOLGA8O, LOC100996255, ULK4P1, ULK4P2, ULK4P3, WHAMMP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035720
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