A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643472



Internal ID6683546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3786940..3791309hg38UCSC Ensembl
Innerchr19:3787440..3790809hg38UCSC Ensembl
Outerchr19:3785940..3792309hg38UCSC Ensembl
chr19:3786938..3791307hg19UCSC Ensembl
Innerchr19:3787438..3790807hg19UCSC Ensembl
Outerchr19:3785938..3792307hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg384370
hg194370
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15977380
SamplesNA18976
Known GenesMATK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643472
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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