A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718187



Internal ID18669782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89141274..89620108hg38UCSC Ensembl
Innerchr15:89684505..90163339hg19UCSC Ensembl
Innerchr15:87485509..87964343hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38478835
hg19478835
hg18478835
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038140
Supporting Variants
Samples
Known GenesABHD2, FANCI, LINC00925, LINC00928, MIR6766, MIR9-3, POLG, RHCG, RLBP1, TICRR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3718187
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