A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15503952



Internal ID5505768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:70147946..70162829hg38UCSC Ensembl
chr16:70181849..70196732hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3814884
hg1914884
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638945
Supporting Variants
SamplesHG01941
Known GenesPDPR
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15503952
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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