A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638370



Internal ID6678468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29686638..29692524hg38UCSC Ensembl
Innerchr16:29686638..29692524hg38UCSC Ensembl
Outerchr16:29686138..29693024hg38UCSC Ensembl
chr16:29697959..29703845hg19UCSC Ensembl
Innerchr16:29697959..29703845hg19UCSC Ensembl
Outerchr16:29697459..29704345hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg385887
hg195887
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15441716, essv15441717
SamplesNA19054, HG02325
Known GenesQPRT
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638370
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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