A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985650



Internal ID12625879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:9262740..10242482hg38UCSC Ensembl
Innerchr10:9304703..10284445hg19UCSC Ensembl
Innerchr10:9344709..10324451hg18UCSC Ensembl
Innerchr10:9344709..10324451hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38979743
hg19979743
hg18979743
hg17979743
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)essv6985650
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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