A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043986



Internal ID18786517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6388351..6414893hg38UCSC Ensembl
Innerchr16:6438352..6464894hg19UCSC Ensembl
Innerchr16:6378353..6404895hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3826543
hg1926543
hg1826543
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557023, nssv3557022
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)nsv1043986
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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