A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999001



Internal ID19158537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:165849594..165983446hg38UCSC Ensembl
Innerchr3:165567382..165701234hg19UCSC Ensembl
Innerchr3:167050076..167183928hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38133853
hg19133853
hg18133853
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4978n100
Supporting Variantsnssv3612684
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999001
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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