A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702429



Internal ID15092395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15669937..15748902hg38UCSC Ensembl
Innerchr19:15780747..15859712hg19UCSC Ensembl
Innerchr19:15641747..15720712hg18UCSC Ensembl
Innerchr19:15641747..15720712hg17UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3878966
hg1978966
hg1878966
hg1778966
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526168
Supporting Variants
Samples
Known GenesCYP4F12, OR10H2, OR10H3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702429
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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