A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585336



Internal ID6972860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16323259..16330818hg38UCSC Ensembl
Innerchr1:16323309..16330768hg38UCSC Ensembl
Outerchr1:16323149..16330928hg38UCSC Ensembl
chr1:16649754..16657313hg19UCSC Ensembl
Innerchr1:16649804..16657263hg19UCSC Ensembl
Outerchr1:16649644..16657423hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg387560
hg197560
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9865174
SamplesHG00732
Known GenesFBXO42
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585336
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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