A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644119



Internal ID7030875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29256709..29275134hg38UCSC Ensembl
Innerchr19:29256709..29275134hg38UCSC Ensembl
Outerchr19:29256209..29275634hg38UCSC Ensembl
chr19:29747616..29766041hg19UCSC Ensembl
Innerchr19:29747616..29766041hg19UCSC Ensembl
Outerchr19:29747116..29766541hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3818426
hg1918426
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16031630
SamplesNA18973
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644119
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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