A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638981



Internal ID7025765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:71832799..71835837hg38UCSC Ensembl
chr16:71866702..71869740hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg383039
hg193039
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15514815, essv15514816, essv15514817
SamplesHG01389, HG01494, HG02235
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638981
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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