A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637716



Internal ID6677817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:5050203..5053230hg38UCSC Ensembl
Innerchr16:5050259..5053175hg38UCSC Ensembl
Outerchr16:5050148..5053286hg38UCSC Ensembl
chr16:5100204..5103231hg19UCSC Ensembl
Innerchr16:5100260..5103176hg19UCSC Ensembl
Outerchr16:5100149..5103287hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg383028
hg193028
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15364000
SamplesHG03202
Known GenesC16orf89
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637716
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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