A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3591041



Internal ID6978369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:62507583..62532882hg38UCSC Ensembl
chr2:62734718..62760017hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg3825300
hg1925300
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv703e214
Supporting Variantsessv10522154, essv10522155, essv10522153
SamplesNA19355, NA19473, NA19351
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3591041
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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