A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16030886



Internal ID6032702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:27755925..27983639hg38UCSC Ensembl
chr19:28246833..28474547hg19UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38227715
hg19227715
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644080
Supporting Variants
SamplesHG02072
Known GenesLINC00662
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16030886
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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