A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3592878



Internal ID6633161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:149814000..149843167hg38UCSC Ensembl
chr2:150670514..150699681hg19UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg3829168
hg1929168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10709118
SamplesNA19355
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3592878
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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