A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633343



Internal ID7020152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100169714..100173819hg38UCSC Ensembl
Innerchr13:100169737..100173797hg38UCSC Ensembl
Outerchr13:100169692..100173842hg38UCSC Ensembl
chr13:100821968..100826073hg19UCSC Ensembl
Innerchr13:100821991..100826051hg19UCSC Ensembl
Outerchr13:100821946..100826096hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg384106
hg194106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14875934
SamplesNA19383
Known GenesPCCA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633343
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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