A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637975



Internal ID7024762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12828594..12841539hg38UCSC Ensembl
Innerchr16:12828594..12841539hg38UCSC Ensembl
Outerchr16:12828094..12842039hg38UCSC Ensembl
chr16:12922451..12935396hg19UCSC Ensembl
Innerchr16:12922451..12935396hg19UCSC Ensembl
Outerchr16:12921951..12935896hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3812946
hg1912946
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15377530
SamplesNA18537
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637975
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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