A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176490



Internal ID15529331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:124464413..124557925hg38UCSC Ensembl
Innerchr9:127226692..127320204hg19UCSC Ensembl
Innerchr9:126266513..126360025hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3893513
hg1993513
hg1893513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615291
Supporting Variants
SamplesHGDP00774
Known GenesNR5A1, NR6A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176490
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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