A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3592480



Internal ID6979807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:131402437..131431447hg38UCSC Ensembl
chr2:132160010..132189020hg19UCSC Ensembl
Cytoband2q21.1
Allele length
AssemblyAllele length
hg3829011
hg1929011
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10674235, essv10674234
SamplesHG02614, HG01600
Known GenesLINC01120
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3592480
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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