A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051331



Internal ID18793862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46395843..46489628hg38UCSC Ensembl
Innerchr10:47059809..47153919hg19UCSC Ensembl
Innerchr10:46479815..46573925hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3893786
hg1994111
hg1894111
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv803n100
Supporting Variantsnssv3513775
Samples
Known GenesHNRNPA1P33, LINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051331
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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