A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14047455



Internal ID2697471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:20876987..20913391hg38UCSC Ensembl
chr11:20898533..20934937hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3836405
hg1936405
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625561
Supporting Variants
SamplesHG02384
Known GenesNELL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14047455
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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