A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041424



Internal ID18783955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112627148..112828670hg38UCSC Ensembl
Innerchr9:115389428..115590950hg19UCSC Ensembl
Innerchr9:114429249..114630771hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38201523
hg19201523
hg18201523
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7701n100
Supporting Variantsnssv3695100, nssv3695099, nssv3695101
Samples
Known GenesINIP, KIAA1958, SNX30
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041424
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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