A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891233



Internal ID19185629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149499939..149617179hg38UCSC Ensembl
Outerchr7:149499939..149617179hg38UCSC Ensembl
Innerchr7:149197030..149314270hg19UCSC Ensembl
Outerchr7:149197030..149314270hg19UCSC Ensembl
Innerchr7:148827963..148945203hg18UCSC Ensembl
Outerchr7:148827963..148945203hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38117241
hg19117241
hg18117241
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783661
Samples
Known GenesZNF767
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891233
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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