A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3591330



Internal ID6631614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:76645385..76757149hg38UCSC Ensembl
chr2:76872511..76984275hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38111765
hg19111765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv707e214
Supporting Variantsessv10550023
SamplesHG01840
Known GenesLRRTM4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3591330
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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