A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003023



Internal ID18745555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:107387583..108187137hg38UCSC Ensembl
Innerchr1:107930205..108729759hg19UCSC Ensembl
Innerchr1:107731728..108531282hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38799555
hg19799555
hg18799555
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv248n100
Supporting Variantsnssv3488006
Samples
Known GenesMIR7852, NTNG1, SLC25A24, VAV3, VAV3-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003023
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