A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644187



Internal ID7030943
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16041384, essv16041386, essv16041385, essv16041383
SamplesHG00536, HG02084, HG01948, HG02113
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644187
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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