A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637699



Internal ID7024489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4652859..4677716hg38UCSC Ensembl
chr16:4702860..4727717hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3824858
hg1924858
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15363716, essv15363717, essv15363715
SamplesHG03479, NA19921, NA19324
Known GenesMGRN1, MIR6769A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637699
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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