A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644130



Internal ID6684198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29966199..29973554hg38UCSC Ensembl
Innerchr19:29966225..29973528hg38UCSC Ensembl
Outerchr19:29966173..29973580hg38UCSC Ensembl
chr19:30457106..30464461hg19UCSC Ensembl
Innerchr19:30457132..30464435hg19UCSC Ensembl
Outerchr19:30457080..30464487hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg387356
hg197356
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16033287
SamplesHG04159
Known GenesURI1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644130
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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