A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045036



Internal ID18787567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:62725022..62891062hg38UCSC Ensembl
Innerchr15:63017221..63183261hg19UCSC Ensembl
Innerchr15:60804513..60970314hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38166041
hg19166041
hg18165802
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3553645
Samples
Known GenesMIR190A, TLN2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045036
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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