A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv748936



Internal ID16042892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:63701880..64962179hg38UCSC Ensembl
Innerchr10:65461640..66721937hg19UCSC Ensembl
Innerchr10:65131646..66391943hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381260300
hg191260298
hg181260298
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551189
Supporting Variants
Samples
Known GenesANXA2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv748936
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