A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638945



Internal ID7025730
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15503952, essv15503954, essv15503950, essv15503951, essv15503956, essv15503955, essv15503953
SamplesNA19794, HG01066, NA20278, NA19719, HG01941, HG03021, HG00707
Known GenesPDPR
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638945
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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