A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15378568



Internal ID4124194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:13576014..13591974hg38UCSC Ensembl
Innerchr16:13576027..13591961hg38UCSC Ensembl
Outerchr16:13576001..13591987hg38UCSC Ensembl
chr16:13669871..13685831hg19UCSC Ensembl
Innerchr16:13669884..13685818hg19UCSC Ensembl
Outerchr16:13669858..13685844hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3815961
hg1915961
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637988
Supporting Variants
SamplesHG03741
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15378568
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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