A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028101



Internal ID19117319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42697890..42825779hg38UCSC Ensembl
Innerchr9:44145340..44273229hg19UCSC Ensembl
Innerchr9:44085336..44213225hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38127890
hg19127890
hg18127890
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7574n100
Supporting Variantsnssv3693053, nssv3693054
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)nsv1028101
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer