A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988087



Internal ID12632843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38459766..38683290hg38UCSC Ensembl
Innerchr9:38459763..38683287hg19UCSC Ensembl
Innerchr9:38449763..38673287hg18UCSC Ensembl
Innerchr9:38449763..38673287hg17UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38223525
hg19223525
hg18223525
hg17223525
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35073
Supporting Variants
SamplesNA12864
Known GenesANKRD18A, FAM201A, FAM95C
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988087
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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