A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614211



Internal ID16054934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:36488264..36622552hg38UCSC Ensembl
Innerchr9:36488261..36622549hg19UCSC Ensembl
Innerchr9:36478261..36612549hg18UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38134289
hg19134289
hg18134289
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1133970
Samples
Known GenesMELK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614211
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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