A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052405



Internal ID18794936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:132336481..132390781hg38UCSC Ensembl
Innerchr10:134149985..134204285hg19UCSC Ensembl
Innerchr10:133999975..134054275hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3854301
hg1954301
hg1854301
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3519229
Samples
Known GenesLRRC27
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052405
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