A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15974448



Internal ID3203603
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643453
Supporting Variants
SamplesHG02811
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15974448
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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