A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570204



Internal ID16357613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:79052074..79102235hg38UCSC Ensembl
Innerchr15:79344416..79394577hg19UCSC Ensembl
Innerchr15:77131471..77181632hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3850162
hg1950162
hg1850162
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv847447
Samples
Known GenesRASGRF1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570204
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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