A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643683



Internal ID6683754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11908685..11910562hg38UCSC Ensembl
Innerchr19:11908735..11910512hg38UCSC Ensembl
Outerchr19:11908635..11910612hg38UCSC Ensembl
chr19:12019500..12021377hg19UCSC Ensembl
Innerchr19:12019550..12021327hg19UCSC Ensembl
Outerchr19:12019450..12021427hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381878
hg191878
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15991073
SamplesHG02624
Known GenesZNF69
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643683
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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