A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25783587



Internal ID18830105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7142651..7182271hg38UCSC Ensembl
Innerchr16:7192652..7232272hg19UCSC Ensembl
Innerchr16:7132653..7172273hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3839621
hg1939621
hg1839621
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892774
Supporting Variants
Samples
Known GenesRBFOX1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=32
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25783587
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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