A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891172



Internal ID18838882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:103796156..104449969hg38UCSC Ensembl
Outerchr7:103796156..104449969hg38UCSC Ensembl
Innerchr7:103436603..104090417hg19UCSC Ensembl
Outerchr7:103436603..104090417hg19UCSC Ensembl
Innerchr7:103223839..103877653hg18UCSC Ensembl
Outerchr7:103223839..103877653hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38653814
hg19653815
hg18653815
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788497
Samples
Known GenesLHFPL3, ORC5, RELN
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891172
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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