A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986937



Internal ID12634039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46188858..46279758hg38UCSC Ensembl
Innerchr10:47560094..47650994hg19UCSC Ensembl
Innerchr10:47030100..47121000hg18UCSC Ensembl
Innerchr10:47030100..47121000hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3890901
hg1990901
hg1890901
hg1790901
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35091
Supporting Variants
SamplesNA18624
Known GenesANTXRLP1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986937
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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