A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551183



Internal ID16338592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:62396351..62464341hg38UCSC Ensembl
Innerchr10:64156110..64224100hg19UCSC Ensembl
Innerchr10:63826116..63894106hg18UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3867991
hg1967991
hg1867991
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174987
SamplesNINDS_56
Known GenesZNF365
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551183
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