A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11030369



Internal ID1032185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:65924258..65950258hg38UCSC Ensembl
chr3:65909933..65935933hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3826001
hg1926001
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596429
Supporting Variants
SamplesNA19035
Known GenesMAGI1, MAGI1-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11030369
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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