A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3656103



Internal ID18607698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:101777539..102110697hg38UCSC Ensembl
Innerchr7:101420819..101753977hg19UCSC Ensembl
Innerchr7:101207539..101540697hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38333159
hg19333159
hg18333159
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020372
Supporting Variants
Samples
Known GenesCUX1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3656103
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