A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989198



Internal ID12972018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:19143845..19543029hg38UCSC Ensembl
Innerchr10:19432774..19831958hg19UCSC Ensembl
Innerchr10:19472780..19871964hg18UCSC Ensembl
Innerchr10:19472780..19871964hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38399185
hg19399185
hg18399185
hg17399185
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 Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989198
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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