A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2752294



Internal ID12985846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28190071..28332482hg38UCSC Ensembl
Innerchr9:28190069..28332480hg19UCSC Ensembl
Innerchr9:28180069..28322480hg18UCSC Ensembl
Innerchr9:28180069..28322480hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38142412
hg19142412
hg18142412
hg17142412
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv259e55
Supporting Variantsessv6989631, essv6982478, essv6982477
SamplesBEC_451
Known GenesLINGO2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv2752294
Frequency
Sample Size771
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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