A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv981213



Internal ID16275169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:170056595..170207178hg38UCSC Ensembl
Innerchr3:169774383..169924966hg19UCSC Ensembl
Innerchr3:171257077..171407660hg18UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38150584
hg19150584
hg18150584
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592506
Supporting Variants
Samples
Known GenesGPR160, PHC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv981213
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