A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550395



Internal ID16337804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34747919..34858486hg38UCSC Ensembl
Innerchr10:35036847..35147414hg19UCSC Ensembl
Innerchr10:35076853..35187420hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38110568
hg19110568
hg18110568
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1032n54
Supporting Variantsnssv1174979
SamplesHGDP00956
Known GenesPARD3, PARD3-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550395
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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