A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570906



Internal ID16011629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101611839..101683568hg38UCSC Ensembl
Innerchr15:102152042..102223771hg19UCSC Ensembl
Innerchr15:99969565..100041294hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3871730
hg1971730
hg1871730
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv851211
Samples
Known GenesTARSL2, TM2D3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570906
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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