A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704523



Internal ID15094489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:110912687..110938984hg38UCSC Ensembl
Innerchr9:113674967..113701264hg19UCSC Ensembl
Innerchr9:112714788..112741085hg18UCSC Ensembl
Innerchr9:110754522..110780819hg17UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3826298
hg1926298
hg1826298
hg1726298
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527998
Supporting Variants
Samples
Known GenesLPAR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704523
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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