A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061465



Internal ID18803996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:3602274..3652130hg38UCSC Ensembl
Innerchr17:3505568..3555424hg19UCSC Ensembl
Innerchr17:3452317..3502173hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3849857
hg1949857
hg1849857
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3085n100
Supporting Variantsnssv3560092, nssv3560093
Samples
Known GenesCTNS, SHPK, TRPV1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061465
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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