A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893653



Internal ID19184473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:7021377..7094901hg38UCSC Ensembl
Outerchr3:7016730..7126014hg38UCSC Ensembl
Innerchr3:7063064..7136588hg19UCSC Ensembl
Outerchr3:7058417..7167701hg19UCSC Ensembl
Innerchr3:7038064..7111588hg18UCSC Ensembl
Outerchr3:7033417..7142701hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38109285
hg19109285
hg18109285
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780395, essv25800501
Samples
Known GenesGRM7
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893653
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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