A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv38n21



Internal ID20131759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15606244..15757643hg38UCSC Ensembl
chr10:15648243..15799642hg19UCSC Ensembl
chr10:15688249..15839648hg18UCSC Ensembl
chr10:15688249..15839648hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38151400
hg19151400
hg18151400
hg17151400
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv521815, nsv521993
Samples
Known GenesITGA8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv38n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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