A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987851



Internal ID12972019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:19154165..19543165hg38UCSC Ensembl
Innerchr10:19443094..19832094hg19UCSC Ensembl
Innerchr10:19483100..19872100hg18UCSC Ensembl
Innerchr10:19483100..19872100hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38389001
hg19389001
hg18389001
hg17389001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750886
Supporting Variants
SamplesBEC_16
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987851
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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