A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644539



Internal ID6684606
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16069723, essv16069724, essv16069722, essv16069721
SamplesHG03100, HG02427, NA19982, HG01375
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644539
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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