A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1132854



Internal ID15986040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:34957866..34958572hg38UCSC Ensembl
Innerchr9:34957863..34958569hg19UCSC Ensembl
Innerchr9:34947863..34948569hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38707
hg19707
hg18707
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614161
Supporting Variants
Samples
Known GenesKIAA1045
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1132854
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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