A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891218



Internal ID19185614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143457550..143479566hg38UCSC Ensembl
Outerchr7:143457550..143479566hg38UCSC Ensembl
Innerchr7:143154643..143176659hg19UCSC Ensembl
Outerchr7:143154643..143176659hg19UCSC Ensembl
Innerchr7:142864765..142886781hg18UCSC Ensembl
Outerchr7:142864765..142886781hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3822017
hg1922017
hg1822017
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799454, essv25798463
Samples
Known GenesEPHA1-AS1, TAS2R41
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891218
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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