A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3642748



Internal ID18941029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:8641604..8725910hg38UCSC Ensembl
Innerchr7:8681234..8765540hg19UCSC Ensembl
Innerchr7:8647759..8732065hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3884307
hg1984307
hg1884307
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019184
Supporting Variants
Samples
Known GenesNXPH1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3642748
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