A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643453



Internal ID7030215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3064669..3073940hg38UCSC Ensembl
Innerchr19:3065169..3073440hg38UCSC Ensembl
Outerchr19:3063669..3074940hg38UCSC Ensembl
chr19:3064667..3073938hg19UCSC Ensembl
Innerchr19:3065167..3073438hg19UCSC Ensembl
Outerchr19:3063667..3074938hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg389272
hg199272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15974450, essv15974448, essv15974449
SamplesHG02811, HG02839, HG03066
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643453
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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