A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891751



Internal ID19186147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6757307..6990209hg38UCSC Ensembl
Outerchr10:6757307..6990209hg38UCSC Ensembl
Innerchr10:6799269..7032171hg19UCSC Ensembl
Outerchr10:6799269..7032171hg19UCSC Ensembl
Innerchr10:6839275..7072177hg18UCSC Ensembl
Outerchr10:6839275..7072177hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38232903
hg19232903
hg18232903
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790829
Samples
Known GenesLINC00706, LINC00707
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891751
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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