A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524574



Internal ID15105181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:4219259..4543307hg38UCSC Ensembl
Innerchr9:4219259..4543307hg19UCSC Ensembl
Innerchr9:4209259..4533307hg18UCSC Ensembl
Innerchr9:4209259..4533307hg17UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38324049
hg19324049
hg18324049
hg17324049
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700530
Samples
Known GenesGLIS3, SLC1A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524574
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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