A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052910



Internal ID18795441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:78316295..78414707hg38UCSC Ensembl
Innerchr15:78608637..78707049hg19UCSC Ensembl
Innerchr15:76395692..76494104hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3898413
hg1998413
hg1898413
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3554590
Samples
Known GenesCRABP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052910
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