A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613955



Internal ID16401364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28049520..28050768hg38UCSC Ensembl
Innerchr9:28049518..28050766hg19UCSC Ensembl
Innerchr9:28039518..28040766hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg381249
hg191249
hg181249
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12622n54
Supporting Variantsnssv1132077
Samples
Known GenesLINGO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613955
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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