A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613957



Internal ID16401366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28049520..28051193hg38UCSC Ensembl
Innerchr9:28049518..28051191hg19UCSC Ensembl
Innerchr9:28039518..28041191hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg381674
hg191674
hg181674
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12623n54
Supporting Variantsnssv1132093, nssv1132083, nssv1132090, nssv1132082, nssv1132086, nssv1132084, nssv1132087, nssv1132089, nssv1132092, nssv1132085, nssv1132081, nssv1132088, nssv1132091, nssv1132094, nssv1132080
Samples
Known GenesLINGO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613957
Frequency
Sample Size17421
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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