A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981711



Internal ID12625898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:9269776..10242096hg38UCSC Ensembl
Innerchr10:9311739..10284059hg19UCSC Ensembl
Innerchr10:9351745..10324065hg18UCSC Ensembl
Innerchr10:9351745..10324065hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38972321
hg19972321
hg18972321
hg17972321
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)essv6981711
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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