A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv417n21



Internal ID22766609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25566105..25575601hg38UCSC Ensembl
chr7:25605725..25615221hg19UCSC Ensembl
chr7:25572250..25581746hg18UCSC Ensembl
chr7:25378965..25388461hg17UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg389497
hg199497
hg189497
hg179497
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv526019, nsv525378
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv417n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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