A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026360



Internal ID18768892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:147291098..147314989hg38UCSC Ensembl
Innerchr7:146988190..147012081hg19UCSC Ensembl
Innerchr7:146619123..146643014hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3823892
hg1923892
hg1823892
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3674228
Samples
Known GenesCNTNAP2, MIR548I4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026360
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