A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633305



Internal ID7020114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98244288..98246345hg38UCSC Ensembl
Innerchr13:98244288..98246345hg38UCSC Ensembl
Outerchr13:98244196..98246440hg38UCSC Ensembl
chr13:98896542..98898599hg19UCSC Ensembl
Innerchr13:98896542..98898599hg19UCSC Ensembl
Outerchr13:98896450..98898694hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg382058
hg192058
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14870641
SamplesNA19904
Known GenesFARP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633305
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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