A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983780



Internal ID12629241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:101295225..101677509hg38UCSC Ensembl
Innerchr10:103054982..103437266hg19UCSC Ensembl
Innerchr10:103044972..103427256hg18UCSC Ensembl
Innerchr10:103044972..103427256hg17UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38382285
hg19382285
hg18382285
hg17382285
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750847
Supporting Variants
SamplesBEC_626
Known GenesBTRC, DPCD, FBXW4, MIR3158-1, MIR3158-2, POLL
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983780
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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