A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv707e214



Internal ID20122130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:76644538..76760877hg38UCSC Ensembl
chr2:76871664..76988003hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38116340
hg19116340
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3591330, esv3591329
SamplesHG01840
Known GenesLRRTM4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv707e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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