A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15364804



Internal ID5366620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:6520040..6521034hg38UCSC Ensembl
Innerchr16:6520069..6521006hg38UCSC Ensembl
Outerchr16:6520012..6521063hg38UCSC Ensembl
chr16:6570041..6571035hg19UCSC Ensembl
Innerchr16:6570070..6571007hg19UCSC Ensembl
Outerchr16:6570013..6571064hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38995
hg19995
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637751
Supporting Variants
SamplesHG03382
Known GenesRBFOX1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15364804
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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