A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14688582



Internal ID821179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:35444436..35469467hg38UCSC Ensembl
chr13:36018573..36043604hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3825032
hg1925032
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3631766
Supporting Variants
SamplesHG00407
Known GenesNBEA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14688582
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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