A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16033289



Internal ID6035105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29995995..29997075hg38UCSC Ensembl
Innerchr19:29996014..29997057hg38UCSC Ensembl
Outerchr19:29995977..29997094hg38UCSC Ensembl
chr19:30486902..30487982hg19UCSC Ensembl
Innerchr19:30486921..30487964hg19UCSC Ensembl
Outerchr19:30486884..30488001hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg381081
hg191081
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644132
Supporting Variants
SamplesHG01795
Known GenesURI1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16033289
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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