A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005121



Internal ID19094338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:173522833..173582391hg38UCSC Ensembl
Innerchr3:173240623..173300181hg19UCSC Ensembl
Innerchr3:174723317..174782875hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3859559
hg1959559
hg1859559
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4986n100
Supporting Variantsnssv3613572, nssv3613574, nssv3613571, nssv3613573, nssv3613570, nssv3613575
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)nsv1005121
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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