A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041519



Internal ID18784050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45991149..46080365hg38UCSC Ensembl
Innerchr10:51515457..51604686hg19UCSC Ensembl
Innerchr10:51185463..51274692hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3889217
hg1989230
hg1889230
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3513132
Samples
Known GenesMSMB, NCOA4, TIMM23
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041519
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