A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988885



Internal ID12631292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:44707669..44856971hg38UCSC Ensembl
Innerchr10:45203117..45352419hg19UCSC Ensembl
Innerchr10:44523123..44672425hg18UCSC Ensembl
Innerchr10:44523123..44672425hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38149303
hg19149303
hg18149303
hg17149303
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750894
Supporting Variants
SamplesBEC_830
Known GenesTMEM72-AS1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988885
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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