A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15365835



Internal ID5367651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:7028745..7038107hg38UCSC Ensembl
Innerchr16:7028745..7038107hg38UCSC Ensembl
Outerchr16:7028245..7038607hg38UCSC Ensembl
chr16:7078746..7088108hg19UCSC Ensembl
Innerchr16:7078746..7088108hg19UCSC Ensembl
Outerchr16:7078246..7088608hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg389363
hg199363
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637790
Supporting Variants
SamplesHG00684
Known GenesRBFOX1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15365835
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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