A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616540



Internal ID6656736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:19192043..19245650hg38UCSC Ensembl
chr8:19049553..19103160hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3853608
hg1953608
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1386e214
Supporting Variantsessv13131073, essv13131072, essv13131075, essv13131074, essv13131071
SamplesNA19214, NA19449, HG01286, HG01182, HG03871
Known GenesLOC100128993
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616540
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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