A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997282



Internal ID19156820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:173497932..173571878hg38UCSC Ensembl
Innerchr3:173215722..173289668hg19UCSC Ensembl
Innerchr3:174698416..174772362hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3873947
hg1973947
hg1873947
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4984n100
Supporting Variantsnssv3612707
Samples
Known GenesNLGN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997282
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