A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15997484



Internal ID5999300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14804503..14812143hg38UCSC Ensembl
Innerchr19:14804503..14812143hg38UCSC Ensembl
Outerchr19:14804176..14812522hg38UCSC Ensembl
chr19:14915315..14922955hg19UCSC Ensembl
Innerchr19:14915315..14922955hg19UCSC Ensembl
Outerchr19:14914988..14923334hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg387641
hg197641
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643752
Supporting Variants
SamplesHG02541
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15997484
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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