A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643594



Internal ID7030353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7814126..7815003hg38UCSC Ensembl
Innerchr19:7814176..7814953hg38UCSC Ensembl
Outerchr19:7814076..7815053hg38UCSC Ensembl
chr19:7879012..7879889hg19UCSC Ensembl
Innerchr19:7879062..7879839hg19UCSC Ensembl
Outerchr19:7878962..7879939hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38878
hg19878
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15987416
SamplesNA18511
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643594
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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