A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3667856



Internal ID18619451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:142236996..142767091hg38UCSC Ensembl
Innerchr7:141583272..142154515hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38530096
hg18571244
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018286
Supporting Variants
Samples
Known GenesLOC730441, MOXD2P, MTRNR2L6, PRSS1, PRSS58
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3667856
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