A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570290



Internal ID16011013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84913115..84922642hg38UCSC Ensembl
Innerchr15:85456346..85465873hg19UCSC Ensembl
Innerchr15:83257350..83266877hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg389528
hg199528
hg189528
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149253
SamplesNINDS_136
Known GenesSLC28A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570290
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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