A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985574



Internal ID12625434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135260209..135426209hg38UCSC Ensembl
Innerchr9:138152055..138318055hg19UCSC Ensembl
Innerchr9:137291876..137457876hg18UCSC Ensembl
Innerchr9:135378000..135544000hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38166001
hg19166001
hg18166001
hg17166001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752284
Supporting Variants
SamplesBEC_22
Known GenesC9orf62
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985574
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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