A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638716



Internal ID6678813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58011317..58046443hg38UCSC Ensembl
chr16:58045221..58080347hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3835127
hg1935127
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15486700
SamplesHG03069
Known GenesMMP15, USB1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638716
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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