A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633344



Internal ID7020153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100201849..100203274hg38UCSC Ensembl
Innerchr13:100201849..100203274hg38UCSC Ensembl
Outerchr13:100201541..100203576hg38UCSC Ensembl
chr13:100854103..100855528hg19UCSC Ensembl
Innerchr13:100854103..100855528hg19UCSC Ensembl
Outerchr13:100853795..100855830hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg381426
hg191426
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14875935
SamplesHG00534
Known GenesPCCA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633344
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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