A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527204



Internal ID15107811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:110883984..110888767hg38UCSC Ensembl
Innerchr9:113646264..113651047hg19UCSC Ensembl
Innerchr9:112686085..112690868hg18UCSC Ensembl
Innerchr9:110725819..110730602hg17UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg384784
hg194784
hg184784
hg174784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703604
Samples
Known GenesLPAR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527204
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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