A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585943



Internal ID6973462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46897535..46950292hg38UCSC Ensembl
chr1:47363207..47415964hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3852758
hg1952758
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9926501, essv9926502
SamplesHG01885, HG03458
Known GenesCYP4A11, CYP4Z2P
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585943
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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