A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005769



Internal ID19094986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:173009410..173039780hg38UCSC Ensembl
Innerchr3:172727200..172757570hg19UCSC Ensembl
Innerchr3:174209894..174240264hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3830371
hg1930371
hg1830371
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3738320
Samples
Known GenesSPATA16
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005769
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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