A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041187



Internal ID18783718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6984267..7088710hg38UCSC Ensembl
Innerchr16:7034268..7138711hg19UCSC Ensembl
Innerchr16:6974269..7078712hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38104444
hg19104444
hg18104444
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3718862
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041187
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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