A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988211



Internal ID12633814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:19524654..19716067hg38UCSC Ensembl
Innerchr10:19813583..20004996hg19UCSC Ensembl
Innerchr10:19853589..20045002hg18UCSC Ensembl
Innerchr10:19853589..20045002hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38191414
hg19191414
hg18191414
hg17191414
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34306
Supporting Variants
SamplesNA18592
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988211
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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