A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643854



Internal ID6683923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19666596..19674464hg38UCSC Ensembl
Innerchr19:19666596..19674464hg38UCSC Ensembl
Outerchr19:19666287..19674708hg38UCSC Ensembl
chr19:19777405..19785273hg19UCSC Ensembl
Innerchr19:19777405..19785273hg19UCSC Ensembl
Outerchr19:19777096..19785517hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg387869
hg197869
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16005741
SamplesHG01171
Known GenesZNF101
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643854
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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