A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041333



Internal ID18783864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7177734..7199211hg38UCSC Ensembl
Innerchr16:7227735..7249212hg19UCSC Ensembl
Innerchr16:7167736..7189213hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3821478
hg1921478
hg1821478
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2717n100
Supporting Variantsnssv3557080
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)nsv1041333
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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