A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3706167



Internal ID19004448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:82453495..82654357hg38UCSC Ensembl
Innerchr10:84213251..84414113hg19UCSC Ensembl
Innerchr10:84203231..84404093hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38200863
hg19200863
hg18200863
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053827
Supporting Variants
Samples
Known GenesNRG3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3706167
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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