A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569974



Internal ID16010697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:74408859..74434772hg38UCSC Ensembl
Innerchr15:74701200..74727113hg19UCSC Ensembl
Innerchr15:72488253..72514166hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3825914
hg1925914
hg1825914
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv845268
Samples
Known GenesMIR6881, SEMA7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569974
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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