A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892760



Internal ID19183580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3273569..3290844hg38UCSC Ensembl
Outerchr16:3273569..3290844hg38UCSC Ensembl
Innerchr16:3323569..3340844hg19UCSC Ensembl
Outerchr16:3323569..3340844hg19UCSC Ensembl
Innerchr16:3263570..3280845hg18UCSC Ensembl
Outerchr16:3263570..3280845hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3817276
hg1917276
hg1817276
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25795977
Samples
Known GenesZNF263
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892760
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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