A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv751943



Internal ID16045899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:81874442..81875329hg38UCSC Ensembl
Innerchr10:83634198..83635085hg19UCSC Ensembl
Innerchr10:83624178..83625065hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38888
hg19888
hg18888
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551681
Supporting Variants
Samples
Known GenesNRG3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv751943
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