A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038791



Internal ID18781322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30212863..30483779hg38UCSC Ensembl
Innerchr15:30505066..30775982hg19UCSC Ensembl
Innerchr15:28292358..28563274hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38270917
hg19270917
hg18270917
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2509n100
Supporting Variantsnssv3546651
Samples
Known GenesCHRFAM7A, DKFZP434L187, LOC101059918
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038791
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