A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633310



Internal ID7020119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98441818..98442590hg38UCSC Ensembl
Innerchr13:98441838..98442570hg38UCSC Ensembl
Outerchr13:98441798..98442610hg38UCSC Ensembl
chr13:99094072..99094844hg19UCSC Ensembl
Innerchr13:99094092..99094824hg19UCSC Ensembl
Outerchr13:99094052..99094864hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg38773
hg19773
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14870677
SamplesNA20762
Known GenesFARP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633310
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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