A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058429



Internal ID19147648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:79169123..79236145hg38UCSC Ensembl
Innerchr17:77165205..77232227hg19UCSC Ensembl
Innerchr17:74676800..74743822hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3867023
hg1967023
hg1867023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3286n100
Supporting Variantsnssv3567830
Samples
Known GenesRBFOX3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058429
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer