A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989497



Internal ID12637253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13323501..13388001hg38UCSC Ensembl
Innerchr9:13323500..13388000hg19UCSC Ensembl
Innerchr9:13313500..13378000hg18UCSC Ensembl
Innerchr9:13313500..13378000hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3864501
hg1964501
hg1864501
hg1764501
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752281
Supporting Variants
SamplesSPC_38
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989497
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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