A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989859



Internal ID12975941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28218502..28332502hg38UCSC Ensembl
Innerchr9:28218500..28332500hg19UCSC Ensembl
Innerchr9:28208500..28322500hg18UCSC Ensembl
Innerchr9:28208500..28322500hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38114001
hg19114001
hg18114001
hg17114001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752292
Supporting Variants
SamplesBEC_628
Known GenesLINGO2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989859
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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