A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043337



Internal ID18785868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6590693..6610156hg38UCSC Ensembl
Innerchr16:6640694..6660157hg19UCSC Ensembl
Innerchr16:6580695..6600158hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3819464
hg1919464
hg1819464
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557027
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)nsv1043337
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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