A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3548846



Internal ID18500441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34403109..34585552hg38UCSC Ensembl
Innerchr15:34695310..34877753hg19UCSC Ensembl
Innerchr15:32482602..32665045hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38182444
hg19182444
hg18182444
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050109
Supporting Variants
Samples
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3548846
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