A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891007



Internal ID19185403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:45653..128206hg38UCSC Ensembl
Outerchr7:45653..128206hg38UCSC Ensembl
Innerchr7:45653..128206hg19UCSC Ensembl
Outerchr7:45653..128206hg19UCSC Ensembl
Innerchr7:140736..223289hg18UCSC Ensembl
Outerchr7:140736..223289hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3882554
hg1982554
hg1882554
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790550
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891007
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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