A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615076



Internal ID16055799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104834004..104834705hg38UCSC Ensembl
Innerchr9:107596285..107596986hg19UCSC Ensembl
Innerchr9:106636106..106636807hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38702
hg19702
hg18702
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12828n54
Supporting Variantsnssv1140868, nssv1140873, nssv1140866, nssv1140871, nssv1140872, nssv1140874, nssv1140867, nssv1140875, nssv1140869, nssv1140870
Samples
Known GenesABCA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615076
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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