A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988449



Internal ID12627217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:132797598..132852920hg38UCSC Ensembl
Innerchr10:134611102..134666424hg19UCSC Ensembl
Innerchr10:134461092..134516414hg18UCSC Ensembl
Innerchr10:134461092..134516414hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3855323
hg1955323
hg1855323
hg1755323
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750852
Supporting Variants
SamplesBEC_466
Known GenesTTC40
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988449
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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