A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv869973



Internal ID15817243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36202819..36265379hg38UCSC Ensembl
Innerchr17:34530219..34609970hg19UCSC Ensembl
Innerchr17:31554332..31634083hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3862561
hg1979752
hg1879752
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574800
Supporting Variants
Samples
Known GenesCCL4L1, CCL4L2, TBC1D3H
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv869973
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