A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518873



Internal ID15446166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:143501855..143518577hg38UCSC Ensembl
Innerchr3:143220697..143237419hg19UCSC Ensembl
Innerchr3:144703387..144720109hg18UCSC Ensembl
Innerchr3:144703395..144720117hg17UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3816723
hg1916723
hg1816723
hg1716723
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696330
Samples
Known GenesSLC9A9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518873
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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