A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037661



Internal ID18780192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7080961..7148477hg38UCSC Ensembl
Innerchr16:7130962..7198478hg19UCSC Ensembl
Innerchr16:7070963..7138479hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3867517
hg1967517
hg1867517
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2715n100
Supporting Variantsnssv3718865, nssv3557075
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)nsv1037661
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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