A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570396



Internal ID16011119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90455896..90565442hg38UCSC Ensembl
Innerchr15:90999128..91108674hg19UCSC Ensembl
Innerchr15:88800132..88909678hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38109547
hg19109547
hg18109547
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv848209
Samples
Known GenesCRTC3, IQGAP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570396
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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