A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv42n21



Internal ID20131763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:61643477..61733966hg38UCSC Ensembl
chr10:63403235..63493724hg19UCSC Ensembl
chr10:63073241..63163730hg18UCSC Ensembl
chr10:63073241..63163730hg17UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3890490
hg1990490
hg1890490
hg1790490
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv528134, nsv527596
Samples
Known GenesC10orf107
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv42n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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