A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1103e214



Internal ID22756997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:66810040..66837550hg38UCSC Ensembl
chr5:66105868..66133378hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3827511
hg1927511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3605319, esv3605320
SamplesHG00640, NA20540, HG01398
Known GenesMAST4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1103e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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