A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv418n21



Internal ID20132139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:34849610..34884725hg38UCSC Ensembl
chr7:34889222..34924337hg19UCSC Ensembl
chr7:34855747..34890862hg18UCSC Ensembl
chr7:34662462..34697577hg17UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3835116
hg1935116
hg1835116
hg1735116
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv528377, nsv516166
Samples
Known GenesNPSR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv418n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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