A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613958



Internal ID16401367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28049757..28051079hg38UCSC Ensembl
Innerchr9:28049755..28051077hg19UCSC Ensembl
Innerchr9:28039755..28041077hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg381323
hg191323
hg181323
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12623n54
Supporting Variantsnssv1132095
Samples
Known GenesLINGO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613958
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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