A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3556326



Internal ID18410716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35170294..35174597hg38UCSC Ensembl
Outerchr19:35169098..35175597hg38UCSC Ensembl
Innerchr19:35661197..35665500hg19UCSC Ensembl
Outerchr19:35660001..35666500hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg386500
hg196500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9755073
Samples
Known GenesFXYD5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3556326
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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