A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv196n21



Internal ID20131917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:77242359..77296076hg38UCSC Ensembl
chr18:74954315..75008032hg19UCSC Ensembl
chr18:73083303..73137020hg18UCSC Ensembl
chr18:73083303..73137020hg17UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3853718
hg1953718
hg1853718
hg1753718
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv518395, nsv523393
Samples
Known GenesGALR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv196n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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