A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633372



Internal ID7020181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:102005659..102017279hg38UCSC Ensembl
Innerchr13:102005659..102017279hg38UCSC Ensembl
Outerchr13:102005336..102017596hg38UCSC Ensembl
chr13:102658009..102669629hg19UCSC Ensembl
Innerchr13:102658009..102669629hg19UCSC Ensembl
Outerchr13:102657686..102669946hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3811621
hg1911621
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14880966
SamplesNA19000
Known GenesFGF14
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633372
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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