A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981769



Internal ID12627216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:132797506..132852506hg38UCSC Ensembl
Innerchr10:134611010..134666010hg19UCSC Ensembl
Innerchr10:134461000..134516000hg18UCSC Ensembl
Innerchr10:134461000..134516000hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3855001
hg1955001
hg1855001
hg1755001
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)essv6981769
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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