A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2752292



Internal ID12985844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28166402..28332502hg38UCSC Ensembl
Innerchr9:28166400..28332500hg19UCSC Ensembl
Innerchr9:28156400..28322500hg18UCSC Ensembl
Innerchr9:28156400..28322500hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38166101
hg19166101
hg18166101
hg17166101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv259e55
Supporting Variantsessv6983798, essv6989392, essv6989859
SamplesBEC_628
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)esv2752292
Frequency
Sample Size771
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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