A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644905



Internal ID7031656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57541493..57543082hg38UCSC Ensembl
Innerchr19:57541493..57543082hg38UCSC Ensembl
Outerchr19:57541377..57543201hg38UCSC Ensembl
chr19:58052861..58054450hg19UCSC Ensembl
Innerchr19:58052861..58054450hg19UCSC Ensembl
Outerchr19:58052745..58054569hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg381590
hg191590
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16107358
SamplesHG02006
Known GenesZNF550
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644905
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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