A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010003



Internal ID18752534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:212770898..212813654hg38UCSC Ensembl
Innerchr1:212944240..212986996hg19UCSC Ensembl
Innerchr1:211010863..211053619hg18UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg3842757
hg1942757
hg1842757
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3489718
Samples
Known GenesNSL1, TATDN3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010003
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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