A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585949



Internal ID6626263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47009618..47041416hg38UCSC Ensembl
Innerchr1:47009618..47041416hg38UCSC Ensembl
Outerchr1:47009118..47041916hg38UCSC Ensembl
chr1:47475290..47507088hg19UCSC Ensembl
Innerchr1:47475290..47507088hg19UCSC Ensembl
Outerchr1:47474790..47507588hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3831799
hg1931799
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9926521
SamplesNA18642
Known GenesCYP4X1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585949
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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