A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14909849



Internal ID2356065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113876772..113933049hg38UCSC Ensembl
chr13:114579745..114636022hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3856278
hg1956278
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633628
Supporting Variants
SamplesHG02087
Known GenesLINC00452, LINC00565
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14909849
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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