A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644898



Internal ID7031649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57216295..57219103hg38UCSC Ensembl
Innerchr19:57216325..57219074hg38UCSC Ensembl
Outerchr19:57216266..57219133hg38UCSC Ensembl
chr19:57727663..57730471hg19UCSC Ensembl
Innerchr19:57727693..57730442hg19UCSC Ensembl
Outerchr19:57727634..57730501hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg382809
hg192809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16107172
SamplesNA20790
Known GenesZNF264
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644898
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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