A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891162



Internal ID19185558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:90556437..90592034hg38UCSC Ensembl
Outerchr7:90556437..90592034hg38UCSC Ensembl
Innerchr7:90185751..90221348hg19UCSC Ensembl
Outerchr7:90185751..90221348hg19UCSC Ensembl
Innerchr7:90023687..90059284hg18UCSC Ensembl
Outerchr7:90023687..90059284hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3835598
hg1935598
hg1835598
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790320, essv25789044, essv25789398
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891162
Frequency
Sample Size3017
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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