A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16041385



Internal ID2347829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33328329..33329075hg38UCSC Ensembl
Innerchr19:33328329..33329075hg38UCSC Ensembl
Outerchr19:33328023..33329368hg38UCSC Ensembl
chr19:33819235..33819981hg19UCSC Ensembl
Innerchr19:33819235..33819981hg19UCSC Ensembl
Outerchr19:33818929..33820274hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38747
hg19747
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644187
Supporting Variants
SamplesHG02084
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16041385
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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