A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644626



Internal ID6684692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:49518636..49522934hg38UCSC Ensembl
Innerchr19:49518676..49522895hg38UCSC Ensembl
Outerchr19:49518597..49522974hg38UCSC Ensembl
chr19:50021893..50026191hg19UCSC Ensembl
Innerchr19:50021933..50026152hg19UCSC Ensembl
Outerchr19:50021854..50026231hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg384299
hg194299
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16075240
SamplesHG04026
Known GenesFCGRT
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644626
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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