A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639477



Internal ID7026257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86122231..86123277hg38UCSC Ensembl
Innerchr16:86122442..86123227hg38UCSC Ensembl
Outerchr16:86122145..86123363hg38UCSC Ensembl
chr16:86155837..86156883hg19UCSC Ensembl
Innerchr16:86156048..86156833hg19UCSC Ensembl
Outerchr16:86155751..86156969hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg381047
hg191047
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15552559, essv15552561, essv15552557, essv15552558, essv15552556, essv15552560, essv15552554, essv15552562, essv15552553, essv15552555
SamplesHG03578, HG03479, HG02703, HG03268, HG01879, HG03428, HG02282, NA19149, NA19147, HG03557
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639477
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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