A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615637



Internal ID16403046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133532712..133539394hg38UCSC Ensembl
Innerchr9:136397834..136404516hg19UCSC Ensembl
Innerchr9:135387655..135394337hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg386683
hg196683
hg186683
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1145448
Samples
Known GenesADAMTSL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615637
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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