A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892833



Internal ID19183653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32128300..32391721hg38UCSC Ensembl
Outerchr16:31990503..32611229hg38UCSC Ensembl
Innerchr16:32139621..32403042hg19UCSC Ensembl
Outerchr16:32001824..32622550hg19UCSC Ensembl
Innerchr16:32047122..32310543hg18UCSC Ensembl
Outerchr16:31909325..32530051hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38620727
hg19620727
hg18620727
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790098, essv25790507, essv25790545, essv25790952, essv25791054, essv25791807, essv25791204, essv25791974, essv25790204, essv25789888, essv25790522, essv25788536, essv25792089, essv25792845, essv25790480, essv25790913, essv25791196, essv25790193, essv25791900, essv25791050, essv25790022, essv25791856, essv25790587
Samples
Known GenesHERC2P4, LOC390705, TP53TG3D
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892833
Frequency
Sample Size3017
Observed Gain23
Observed Loss0
Observed Complex0
Frequencyn/a


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