A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3593267



Internal ID6633547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:166935598..167000742hg38UCSC Ensembl
chr2:167792108..167857252hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3865145
hg1965145
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10750897
SamplesHG00589
Known GenesXIRP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3593267
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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