A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788899



Internal ID19160967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:31566892..31618828hg38UCSC Ensembl
Innerchr16:31578213..31630149hg19UCSC Ensembl
Innerchr16:31485714..31537650hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3851937
hg1951937
hg1851937
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892828
Supporting Variants
Samples
Known GenesYBX3P1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=12
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788899
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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