A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637839



Internal ID6677939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8681250..8681899hg38UCSC Ensembl
Innerchr16:8681262..8681888hg38UCSC Ensembl
Outerchr16:8681239..8681911hg38UCSC Ensembl
chr16:8775107..8775756hg19UCSC Ensembl
Innerchr16:8775119..8775745hg19UCSC Ensembl
Outerchr16:8775096..8775768hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38650
hg19650
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15371913, essv15371914, essv15371915
SamplesNA19679, HG03742, HG00110
Known GenesABAT
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637839
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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