A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14870641



Internal ID6300557
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633305
Supporting Variants
SamplesNA19904
Known GenesFARP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14870641
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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