A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3560100



Internal ID18511695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:3602274..3654147hg38UCSC Ensembl
Innerchr17:3505568..3557441hg19UCSC Ensembl
Innerchr17:3452317..3504190hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3851874
hg1951874
hg1851874
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059749
Supporting Variants
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)nssv3560100
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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