A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639337



Internal ID7026119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81636931..81642472hg38UCSC Ensembl
Innerchr16:81636948..81642456hg38UCSC Ensembl
Outerchr16:81636915..81642489hg38UCSC Ensembl
chr16:81670536..81676077hg19UCSC Ensembl
Innerchr16:81670553..81676061hg19UCSC Ensembl
Outerchr16:81670520..81676094hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg385542
hg195542
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15537865, essv15537866, essv15537863, essv15537864, essv15537861, essv15537862
SamplesHG02661, NA20892, HG02657, HG03940, HG02685, HG03022
Known GenesCMIP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639337
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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