A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638038



Internal ID7024824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15602116..15633311hg38UCSC Ensembl
chr16:15695973..15727168hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3831196
hg1931196
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15385635, essv15385636, essv15385634
SamplesHG00334, HG03072, HG03890
Known GenesKIAA0430, MIR6506
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638038
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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