A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047496



Internal ID18790027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:92869548..92932648hg38UCSC Ensembl
Innerchr15:93412778..93475878hg19UCSC Ensembl
Innerchr15:91213782..91276882hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3863101
hg1963101
hg1863101
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2660n100
Supporting Variantsnssv3555231
Samples
Known GenesCHD2, LOC100507217, MIR3175
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047496
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