A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574797



Internal ID16015520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36202819..36217165hg38UCSC Ensembl
Innerchr17:34530219..34544619hg19UCSC Ensembl
Innerchr17:31554332..31568732hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3814347
hg1914401
hg1814401
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5546n54
Supporting Variantsnssv869967, nssv869969, nssv869966, nssv869968, nssv869970
Samples
Known GenesCCL4L1, CCL4L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574797
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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