A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613726



Internal ID16401135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:18676165..18709332hg38UCSC Ensembl
Innerchr9:18676163..18709330hg19UCSC Ensembl
Innerchr9:18666163..18699330hg18UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3833168
hg1933168
hg1833168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1130782
Samples
Known GenesADAMTSL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613726
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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