A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2752226



Internal ID12985778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675575..136850575hg38UCSC Ensembl
Innerchr8:137687818..137862818hg19UCSC Ensembl
Innerchr8:137757000..137932000hg18UCSC Ensembl
Innerchr8:137757000..137932000hg17UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38175001
hg19175001
hg18175001
hg17175001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv252e55
Supporting Variantsessv6989449, essv6990008, essv6984707, essv6984708, essv6984709
SamplesSPC_167
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv2752226
Frequency
Sample Size771
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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