A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892784



Internal ID19183604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:8245405..8271928hg38UCSC Ensembl
Outerchr16:8245405..8271928hg38UCSC Ensembl
Innerchr16:8295407..8321930hg19UCSC Ensembl
Outerchr16:8295407..8321930hg19UCSC Ensembl
Innerchr16:8235408..8261931hg18UCSC Ensembl
Outerchr16:8235408..8261931hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3826524
hg1926524
hg1826524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779030
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892784
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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