A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062593



Internal ID19151812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:35357088..35430104hg38UCSC Ensembl
Innerchr17:33684107..33757123hg19UCSC Ensembl
Innerchr17:30708220..30781236hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3873017
hg1973017
hg1873017
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3142n100
Supporting Variantsnssv3561075, nssv3561076
Samples
Known GenesSLFN11, SLFN12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062593
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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