A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043952



Internal ID18786483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6739940..6785871hg38UCSC Ensembl
Innerchr16:6789941..6835872hg19UCSC Ensembl
Innerchr16:6729942..6775873hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3845932
hg1945932
hg1845932
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2707n100
Supporting Variantsnssv3718850
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)nsv1043952
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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