A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779976



Internal ID19182605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84492337..84506132hg38UCSC Ensembl
Innerchr16:84525943..84539738hg19UCSC Ensembl
Innerchr16:83083444..83097239hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3813796
hg1913796
hg1813796
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892929
Supporting Variants
Samples
Known GenesTLDC1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779976
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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