A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv179n21



Internal ID22766371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:40231788..40248785hg38UCSC Ensembl
chr17:38388040..38405037hg19UCSC Ensembl
chr17:35641566..35658563hg18UCSC Ensembl
chr17:35641566..35658563hg17UCSC Ensembl
Cytoband17q21.1
Allele length
AssemblyAllele length
hg3816998
hg1916998
hg1816998
hg1716998
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv525961, nsv522863
Samples
Known GenesWIPF2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv179n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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