A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615619



Internal ID16403028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133256028..133257183hg38UCSC Ensembl
Innerchr9:136131415..136132570hg19UCSC Ensembl
Innerchr9:135121236..135122391hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg381156
hg191156
hg181156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12932n54
Supporting Variantsnssv1145406
Samples
Known GenesABO
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615619
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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