A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049407



Internal ID19138626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:91106094..91150097hg38UCSC Ensembl
Innerchr10:92865851..92909854hg19UCSC Ensembl
Innerchr10:92855831..92899834hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3844004
hg1944004
hg1844004
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv953n100
Supporting Variantsnssv3520938, nssv3512437
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)nsv1049407
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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