A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043386



Internal ID18785917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34403109..34576683hg38UCSC Ensembl
Innerchr15:34695310..34868884hg19UCSC Ensembl
Innerchr15:32482602..32656176hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38173575
hg19173575
hg18173575
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2554n100
Supporting Variantsnssv3548842
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)nsv1043386
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