A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066300



Internal ID19155519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:66514292..66595345hg38UCSC Ensembl
Innerchr17:64510410..64591463hg19UCSC Ensembl
Innerchr17:61940872..62021925hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3881054
hg1981054
hg1881054
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3275n100
Supporting Variantsnssv3567737
Samples
Known GenesPRKCA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066300
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