A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3661319



Internal ID18959600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:54173290..54236478hg38UCSC Ensembl
Innerchr7:54240983..54304171hg19UCSC Ensembl
Innerchr7:54208477..54271665hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3863189
hg1963189
hg1863189
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031162
Supporting Variants
Samples
Known GenesHPVC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3661319
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer