A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551578



Internal ID15992301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79242612..79243739hg38UCSC Ensembl
Innerchr10:81002369..81003496hg19UCSC Ensembl
Innerchr10:80672375..80673502hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg381128
hg191128
hg181128
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1277n54
Supporting Variantsnssv751759, nssv751760, nssv751761
Samples
Known GenesZMIZ1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551578
Frequency
Sample Size17421
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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