A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615075



Internal ID16055798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104833924..104836459hg38UCSC Ensembl
Innerchr9:107596205..107598740hg19UCSC Ensembl
Innerchr9:106636026..106638561hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg382536
hg192536
hg182536
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1140865
Samples
Known GenesABCA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615075
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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