A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988064



Internal ID12979274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:10547900..10581500hg38UCSC Ensembl
Innerchr9:10547900..10581500hg19UCSC Ensembl
Innerchr9:10537900..10571500hg18UCSC Ensembl
Innerchr9:10537900..10571500hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3833601
hg1933601
hg1833601
hg1733601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34558
Supporting Variants
SamplesNA12752
Known GenesPTPRD
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988064
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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