A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644315



Internal ID7031071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38968121..39015299hg38UCSC Ensembl
Innerchr19:38968621..39014799hg38UCSC Ensembl
Outerchr19:38967121..39016299hg38UCSC Ensembl
chr19:39458761..39505939hg19UCSC Ensembl
Innerchr19:39459261..39505439hg19UCSC Ensembl
Outerchr19:39457761..39506939hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3847179
hg1947179
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16054318
SamplesHG02153
Known GenesFBXO17
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644315
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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