A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891027



Internal ID19185423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:4928494..4939705hg38UCSC Ensembl
Outerchr7:4928494..4939705hg38UCSC Ensembl
Innerchr7:4968125..4979336hg19UCSC Ensembl
Outerchr7:4968125..4979336hg19UCSC Ensembl
Innerchr7:4934651..4945862hg18UCSC Ensembl
Outerchr7:4934651..4945862hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3811212
hg1911212
hg1811212
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800713
Samples
Known GenesMMD2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891027
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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