A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978175



Internal ID12981540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1826476..1867326hg38UCSC Ensembl
Innerchr10:1868670..1909520hg19UCSC Ensembl
Innerchr10:1858670..1899520hg18UCSC Ensembl
Innerchr10:1858670..1899520hg17UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3840851
hg1940851
hg1840851
hg1740851
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34498
Supporting Variants
SamplesNA18974
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978175
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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