A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569401



Internal ID16010124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:50586433..50613583hg38UCSC Ensembl
Innerchr15:50878630..50905780hg19UCSC Ensembl
Innerchr15:48665922..48693072hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3827151
hg1927151
hg1827151
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv842977
Samples
Known GenesTRPM7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569401
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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