A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv497n21



Internal ID20132218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127870863..127898531hg38UCSC Ensembl
chr9:130633142..130660810hg19UCSC Ensembl
chr9:129672963..129700631hg18UCSC Ensembl
chr9:127712696..127740364hg17UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3827669
hg1927669
hg1827669
hg1727669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv517661, nsv518602
Samples
Known GenesAK1, ST6GALNAC6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv497n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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