A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644497



Internal ID6684564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45085975..45092273hg38UCSC Ensembl
Innerchr19:45086025..45092223hg38UCSC Ensembl
Outerchr19:45085891..45092357hg38UCSC Ensembl
chr19:45589233..45595531hg19UCSC Ensembl
Innerchr19:45589283..45595481hg19UCSC Ensembl
Outerchr19:45589149..45595615hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg386299
hg196299
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16066416
SamplesNA11894
Known GenesGEMIN7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644497
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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