A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15370944



Internal ID5372760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8522841..8529505hg38UCSC Ensembl
Innerchr16:8522844..8529502hg38UCSC Ensembl
Outerchr16:8522838..8529508hg38UCSC Ensembl
chr16:8572843..8579507hg19UCSC Ensembl
Innerchr16:8572846..8579504hg19UCSC Ensembl
Outerchr16:8572840..8579510hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg386665
hg196665
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637835
Supporting Variants
SamplesHG02810
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15370944
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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