A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891138



Internal ID19185534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:67044615..67262802hg38UCSC Ensembl
Outerchr7:67044615..67262802hg38UCSC Ensembl
Innerchr7:66509602..66727789hg19UCSC Ensembl
Outerchr7:66509602..66727789hg19UCSC Ensembl
Innerchr7:66147037..66365224hg18UCSC Ensembl
Outerchr7:66147037..66365224hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38218188
hg19218188
hg18218188
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792701
Samples
Known GenesMIR4650-1, MIR4650-2, TYW1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891138
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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