A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988214



Internal ID12633858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7014035..7031092hg38UCSC Ensembl
Innerchr16:7064036..7081093hg19UCSC Ensembl
Innerchr16:7004037..7021094hg18UCSC Ensembl
Innerchr16:7004037..7021094hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3817058
hg1917058
hg1817058
hg1717058
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34350
Supporting Variants
SamplesNA18593
Known GenesRBFOX1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988214
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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