A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639338



Internal ID7026120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81643560..81648580hg38UCSC Ensembl
Innerchr16:81643595..81648546hg38UCSC Ensembl
Outerchr16:81643526..81648615hg38UCSC Ensembl
chr16:81677165..81682185hg19UCSC Ensembl
Innerchr16:81677200..81682151hg19UCSC Ensembl
Outerchr16:81677131..81682220hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg385021
hg195021
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15537868, essv15537867
SamplesHG02661, HG02646
Known GenesCMIP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639338
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer