A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044381



Internal ID18786912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112620973..112828670hg38UCSC Ensembl
Innerchr9:115383253..115590950hg19UCSC Ensembl
Innerchr9:114423074..114630771hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38207698
hg19207698
hg18207698
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7701n100
Supporting Variantsnssv3695084, nssv3695069, nssv3695098, nssv3695089, nssv3695079, nssv3695097, nssv3695095, nssv3695092, nssv3695088, nssv3695085, nssv3695074, nssv3695078, nssv3695094, nssv3695080, nssv3695082, nssv3695077, nssv3695073, nssv3695093, nssv3695081, nssv3695071, nssv3695076, nssv3695072, nssv3695090, nssv3695083, nssv3695087, nssv3695070, nssv3695096, nssv3695075, nssv3695091, nssv3695068, nssv3695086
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)nsv1044381
Frequency
Sample Size29084
Observed Gain31
Observed Loss0
Observed Complex0
Frequencyn/a


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