A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574462



Internal ID16361871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15544050..15708181hg38UCSC Ensembl
Innerchr17:15447364..15611495hg19UCSC Ensembl
Innerchr17:15388089..15552220hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38164132
hg19164132
hg18164132
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149748
SamplesHGDP00800
Known GenesCDRT1, TRIM16, TVP23C, TVP23C-CDRT4, ZNF286A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574462
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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