A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2752289



Internal ID12639155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21361958..21499625hg38UCSC Ensembl
Innerchr9:21361957..21499624hg19UCSC Ensembl
Innerchr9:21351957..21489624hg18UCSC Ensembl
Innerchr9:21351957..21489624hg17UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38137668
hg19137668
hg18137668
hg17137668
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6986186, essv6988542
SamplesBEC_451
Known GenesIFNA1, IFNA13, IFNA2, IFNA8, IFNE, MIR31HG
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv2752289
Frequency
Sample Size771
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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