A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038313



Internal ID18780844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90092950..90120822hg38UCSC Ensembl
Innerchr15:90636182..90664054hg19UCSC Ensembl
Innerchr15:88437186..88465058hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3827873
hg1927873
hg1827873
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555197
Samples
Known GenesIDH2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038313
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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