A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643433



Internal ID7030195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2683165..2689626hg38UCSC Ensembl
Innerchr19:2683315..2689476hg38UCSC Ensembl
Outerchr19:2683015..2689776hg38UCSC Ensembl
chr19:2683163..2689624hg19UCSC Ensembl
Innerchr19:2683313..2689474hg19UCSC Ensembl
Outerchr19:2683013..2689774hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg386462
hg196462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15969587
SamplesHG02064
Known GenesGNG7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643433
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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