A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14848249



Internal ID3753202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90936411..91050754hg38UCSC Ensembl
chr13:91588665..91703008hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38114344
hg19114344
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633143
Supporting Variants
SamplesHG03382
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14848249
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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