A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv180n21



Internal ID22766372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:54755970..54827165hg38UCSC Ensembl
chr17:52833331..52904526hg19UCSC Ensembl
chr17:50188330..50259525hg18UCSC Ensembl
chr17:50188330..50259525hg17UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3871196
hg1971196
hg1871196
hg1771196
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv525424, nsv525657
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv180n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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