A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv407n21



Internal ID22766599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:13602049..13643455hg38UCSC Ensembl
chr7:13641674..13683080hg19UCSC Ensembl
chr7:13608199..13649605hg18UCSC Ensembl
chr7:13414914..13456320hg17UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3841407
hg1941407
hg1841407
hg1741407
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv522998, nsv520006
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv407n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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