A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988430



Internal ID12625740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:24131802..24423202hg38UCSC Ensembl
Innerchr9:24131800..24423200hg19UCSC Ensembl
Innerchr9:24121800..24413200hg18UCSC Ensembl
Innerchr9:24121800..24413200hg17UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38291401
hg19291401
hg18291401
hg17291401
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752290
Supporting Variants
SamplesBEC_309
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988430
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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