A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029476



Internal ID19118695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:57193213..57960277hg38UCSC Ensembl
Innerchr7:57260920..58019983hg19UCSC Ensembl
Innerchr7:57264862..58023925hg18UCSC Ensembl
Cytoband7p11.1
Allele length
AssemblyAllele length
hg38767065
hg19759064
hg18759064
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6369n100
Supporting Variantsnssv3752978
Samples
Known GenesMIR3147, ZNF716
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029476
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