A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022929



Internal ID19112146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155191409..155229466hg38UCSC Ensembl
Innerchr7:154983119..155021176hg19UCSC Ensembl
Innerchr7:154614052..154652109hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3838058
hg1938058
hg1838058
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6765n100
Supporting Variantsnssv3674686
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)nsv1022929
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