A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048948



Internal ID19138167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76586021..76617690hg38UCSC Ensembl
Innerchr15:76878362..76910031hg19UCSC Ensembl
Innerchr15:74665417..74697086hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3831670
hg1931670
hg1831670
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2629n100
Supporting Variantsnssv3554501, nssv3718069
Samples
Known GenesSCAPER
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048948
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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