A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043990



Internal ID18786521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47185851..47278335hg38UCSC Ensembl
Innerchr10:48461027..48553511hg19UCSC Ensembl
Innerchr10:48081033..48173517hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3892485
hg1992485
hg1892485
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3507914
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)nsv1043990
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