A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638009



Internal ID7024795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14518485..14520506hg38UCSC Ensembl
Innerchr16:14518520..14520471hg38UCSC Ensembl
Outerchr16:14518450..14520541hg38UCSC Ensembl
chr16:14612342..14614363hg19UCSC Ensembl
Innerchr16:14612377..14614328hg19UCSC Ensembl
Outerchr16:14612307..14614398hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg382022
hg192022
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15379393
SamplesHG03195
Known GenesPARN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638009
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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