A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3670382



Internal ID18621977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143549301..143780696hg38UCSC Ensembl
Innerchr7:143246394..143477789hg19UCSC Ensembl
Innerchr7:142956516..143108722hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38231396
hg19231396
hg18152207
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024360
Supporting Variants
Samples
Known GenesCTAGE15, CTAGE6, FAM115C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3670382
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