A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637903



Internal ID6678003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10495286..10528746hg38UCSC Ensembl
chr16:10589143..10622603hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3833461
hg1933461
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15373028
SamplesHG01260
Known GenesEMP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637903
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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