A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3587236



Internal ID6974663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:113268339..113391162hg38UCSC Ensembl
chr1:113810961..113933784hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38122824
hg19122824
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10079197
SamplesNA18523
Known GenesMAGI3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3587236
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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