A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981710



Internal ID12625899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:9241541..10242531hg38UCSC Ensembl
Innerchr10:9283504..10284494hg19UCSC Ensembl
Innerchr10:9323510..10324500hg18UCSC Ensembl
Innerchr10:9323510..10324500hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381000991
hg191000991
hg181000991
hg171000991
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750976
Supporting Variants
SamplesBEC_328
Known GenesLINC00709
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981710
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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