A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613725



Internal ID16401134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:18651446..18663545hg38UCSC Ensembl
Innerchr9:18651444..18663543hg19UCSC Ensembl
Innerchr9:18641444..18653543hg18UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3812100
hg1912100
hg1812100
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1130781
Samples
Known GenesADAMTSL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613725
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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