A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575852



Internal ID16363261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:63009712..63155117hg38UCSC Ensembl
Innerchr17:61087073..61232478hg19UCSC Ensembl
Innerchr17:58440805..58586210hg18UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38145406
hg19145406
hg18145406
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5742n54
Supporting Variantsnssv1149782
SamplesHGDP00647
Known GenesMIR548W, TANC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575852
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