A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv726564



Internal ID16020520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:159045530..159048132hg38UCSC Ensembl
Innerchr1:159015320..159017922hg19UCSC Ensembl
Innerchr1:157281944..157284546hg18UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg382603
hg192603
hg182603
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv548049
Supporting Variants
Samples
Known GenesIFI16
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv726564
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