A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703604



Internal ID15093570
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527204
Supporting Variants
Samples
Known GenesLPAR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703604
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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