A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3590432



Internal ID6977761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:39476271..39535976hg38UCSC Ensembl
chr2:39703412..39763117hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3859706
hg1959706
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10470757
SamplesHG02070
Known GenesLOC728730
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3590432
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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