A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569703



Internal ID16010426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:64756110..64930560hg38UCSC Ensembl
Innerchr15:65048309..65222758hg19UCSC Ensembl
Innerchr15:62835362..63009811hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38174451
hg19174450
hg18174450
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv843970
Samples
Known GenesANKDD1A, MIR1272, PIF1, PLEKHO2, RBPMS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569703
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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