A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15375348



Internal ID3267773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11580306..11641150hg38UCSC Ensembl
Innerchr16:11580306..11641150hg38UCSC Ensembl
Outerchr16:11579806..11641650hg38UCSC Ensembl
chr16:11674162..11735006hg19UCSC Ensembl
Innerchr16:11674162..11735006hg19UCSC Ensembl
Outerchr16:11673662..11735506hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3860845
hg1960845
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637930
Supporting Variants
SamplesHG02885
Known GenesLITAF
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15375348
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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