A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637902



Internal ID7024690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10493976..10501693hg38UCSC Ensembl
Innerchr16:10493976..10501693hg38UCSC Ensembl
Outerchr16:10493476..10502193hg38UCSC Ensembl
chr16:10587833..10595550hg19UCSC Ensembl
Innerchr16:10587833..10595550hg19UCSC Ensembl
Outerchr16:10587333..10596050hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg387718
hg197718
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15373027
SamplesHG02087
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637902
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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