A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615084



Internal ID16055807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104849546..104873588hg38UCSC Ensembl
Innerchr9:107611827..107635869hg19UCSC Ensembl
Innerchr9:106651648..106675690hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3824043
hg1924043
hg1824043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1140895, nssv1140893, nssv1140894
Samples
Known GenesABCA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615084
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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