A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv875849



Internal ID16169805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:66414797..66514292hg38UCSC Ensembl
Innerchr17:64410915..64510410hg19UCSC Ensembl
Innerchr17:61841377..61940872hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3899496
hg1999496
hg1899496
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575897
Supporting Variants
Samples
Known GenesPRKCA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv875849
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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