A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988542



Internal ID12973811
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 StatusS
Merged Variantsesv2752289
Supporting Variants
SamplesBEC_451
Known GenesIFNA1, IFNA13, IFNA2, IFNA8, IFNE, MIR31HG
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988542
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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