A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892929



Internal ID19183749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84492337..84506132hg38UCSC Ensembl
Outerchr16:84492337..84506132hg38UCSC Ensembl
Innerchr16:84525943..84539738hg19UCSC Ensembl
Outerchr16:84525943..84539738hg19UCSC Ensembl
Innerchr16:83083444..83097239hg18UCSC Ensembl
Outerchr16:83083444..83097239hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3813796
hg1913796
hg1813796
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779976
Samples
Known GenesTLDC1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892929
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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