A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025219



Internal ID19114437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:97756249..97774916hg38UCSC Ensembl
Innerchr7:97385561..97404228hg19UCSC Ensembl
Innerchr7:97223497..97242164hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3818668
hg1918668
hg1818668
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6535n100
Supporting Variantsnssv3755446
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025219
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