A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608658



Internal ID16049381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143095565..143239150hg38UCSC Ensembl
Innerchr7:142792658..142936243hg19UCSC Ensembl
Innerchr7:142502780..142646365hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38143586
hg19143586
hg18143586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11660n54
Supporting Variantsnssv1096485
Samples
Known GenesPIP, TAS2R39, TAS2R40
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608658
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