A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044686



Internal ID19133905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:44197336..44405284hg38UCSC Ensembl
Innerchr15:44489534..44697482hg19UCSC Ensembl
Innerchr15:42276826..42484774hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38207949
hg19207949
hg18207949
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2587n100
Supporting Variantsnssv3552336
Samples
Known GenesCASC4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044686
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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