A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv747366



Internal ID15694636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46389706..46558889hg38UCSC Ensembl
Innerchr10:46990728..47160061hg19UCSC Ensembl
Innerchr10:46410734..46580067hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38169184
hg19169334
hg18169334
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550723
Supporting Variants
Samples
Known GenesANXA8, GPRIN2, HNRNPA1P33, LINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv747366
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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