A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032050



Internal ID19121272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:158635368..158687756hg38UCSC Ensembl
Innerchr7:158428060..158480448hg19UCSC Ensembl
Innerchr7:158120821..158173209hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3852389
hg1952389
hg1852389
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3674763
Samples
Known GenesNCAPG2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032050
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