A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891120



Internal ID19185516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:61101821..62977911hg38UCSC Ensembl
Innerchr7:61286246..62241041hg19UCSC Ensembl
Outerchr7:61084546..62438289hg19UCSC Ensembl
Innerchr7:61290188..61878476hg18UCSC Ensembl
Outerchr7:61088488..62075724hg18UCSC Ensembl
Cytoband7q11.1
Allele length
AssemblyAllele length
hg381876091
hg191353744
hg18987237
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789706, essv25789693, essv25790120, essv25789802, essv25789650, essv25790076, essv25790731
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891120
Frequency
Sample Size3017
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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