A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3518550



Internal ID18816831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46574569..46595134hg38UCSC Ensembl
Innerchr10:46954483..46975048hg19UCSC Ensembl
Innerchr10:46374489..46395054hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3820566
hg1920566
hg1820566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047376
Supporting Variants
Samples
Known GenesSYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3518550
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