A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3590372



Internal ID6977701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:35730688..35871372hg38UCSC Ensembl
chr2:35955754..36096438hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38140685
hg19140685
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10460272, essv10460270, essv10460271, essv10460273
SamplesHG01766, HG02733, HG03695, NA20870
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3590372
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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