A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16069724



Internal ID6071540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46873736..46876632hg38UCSC Ensembl
Innerchr19:46874236..46876132hg38UCSC Ensembl
Outerchr19:46872736..46877632hg38UCSC Ensembl
chr19:47376993..47379889hg19UCSC Ensembl
Innerchr19:47377493..47379389hg19UCSC Ensembl
Outerchr19:47375993..47380889hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg382897
hg192897
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644539
Supporting Variants
SamplesNA19982
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16069724
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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