A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16033287



Internal ID6035103
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644130
Supporting Variants
SamplesHG04159
Known GenesURI1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16033287
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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