A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980362



Internal ID12978262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7666090..7781370hg38UCSC Ensembl
Innerchr9:7666090..7781370hg19UCSC Ensembl
Innerchr9:7656090..7771370hg18UCSC Ensembl
Innerchr9:7656090..7771370hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38115281
hg19115281
hg18115281
hg17115281
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34566
Supporting Variants
SamplesNA07345
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980362
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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