A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615291



Internal ID16056014
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 StatusM
Merged Variants
Supporting Variantsnssv1176490
SamplesHGDP00774
Known GenesNR5A1, NR6A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615291
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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