A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16027790



Internal ID6029606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:27348171..28149207hg38UCSC Ensembl
chr19:27839079..28640114hg19UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38801037
hg19801036
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644065
Supporting Variants
SamplesHG03900
Known GenesLINC00662
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16027790
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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