A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986186



Internal ID12627120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21407401..21499601hg38UCSC Ensembl
Innerchr9:21407400..21499600hg19UCSC Ensembl
Innerchr9:21397400..21489600hg18UCSC Ensembl
Innerchr9:21397400..21489600hg17UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3892201
hg1992201
hg1892201
hg1792201
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752289
Supporting Variants
SamplesBEC_451
Known GenesIFNA1, IFNA8, IFNE, MIR31HG
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986186
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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