A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638906



Internal ID7025691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68392012..68393093hg38UCSC Ensembl
Innerchr16:68392056..68393049hg38UCSC Ensembl
Outerchr16:68391968..68393137hg38UCSC Ensembl
chr16:68425915..68426996hg19UCSC Ensembl
Innerchr16:68425959..68426952hg19UCSC Ensembl
Outerchr16:68425871..68427040hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg381082
hg191082
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15501627
SamplesHG02239
Known GenesSMPD3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638906
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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