A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892873



Internal ID19183693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:64123913..64200550hg38UCSC Ensembl
Outerchr16:64123913..64200550hg38UCSC Ensembl
Innerchr16:64157817..64234454hg19UCSC Ensembl
Outerchr16:64157817..64234454hg19UCSC Ensembl
Innerchr16:62715318..62791955hg18UCSC Ensembl
Outerchr16:62715318..62791955hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3876638
hg1976638
hg1876638
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800666
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892873
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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