A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25778905



Internal ID18822184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6872577..7019055hg38UCSC Ensembl
Innerchr16:6922578..7069056hg19UCSC Ensembl
Innerchr16:6862579..7009057hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38146479
hg19146479
hg18146479
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892776
Supporting Variants
Samples
Known GenesRBFOX1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=58
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25778905
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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