A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643841



Internal ID6683910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18587326..18591044hg38UCSC Ensembl
Innerchr19:18587336..18591035hg38UCSC Ensembl
Outerchr19:18587317..18591054hg38UCSC Ensembl
chr19:18698136..18701854hg19UCSC Ensembl
Innerchr19:18698146..18701845hg19UCSC Ensembl
Outerchr19:18698127..18701864hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg383719
hg193719
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16003964
SamplesHG02272
Known GenesC19orf60
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643841
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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