A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891089



Internal ID19185485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:24704690..24729781hg38UCSC Ensembl
Outerchr7:24704690..24729781hg38UCSC Ensembl
Innerchr7:24744309..24769400hg19UCSC Ensembl
Outerchr7:24744309..24769400hg19UCSC Ensembl
Innerchr7:24710834..24735925hg18UCSC Ensembl
Outerchr7:24710834..24735925hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3825092
hg1925092
hg1825092
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782375
Samples
Known GenesDFNA5
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891089
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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