A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633139



Internal ID7019949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90883943..90926847hg38UCSC Ensembl
chr13:91536197..91579101hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3842905
hg1942905
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14848215, essv14848217, essv14848216
SamplesNA19332, HG03126, HG03382
Known GenesLINC00410
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633139
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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