A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638982



Internal ID7025766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:71832799..71835837hg38UCSC Ensembl
chr16:71866702..71869740hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg383039
hg193039
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15514822, essv15514820, essv15514819, essv15514818, essv15514821, essv15514823
SamplesHG00096, HG03792, HG01673, HG02943, NA20534, HG02941
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638982
Frequency
Sample Size2504
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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