A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569236



Internal ID16356645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:42104084..42125887hg38UCSC Ensembl
Innerchr15:42396282..42418085hg19UCSC Ensembl
Innerchr15:40183574..40205377hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3821804
hg1921804
hg1821804
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149588
SamplesNINDS_272
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569236
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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