A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv427n21



Internal ID22766619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:111173752..111472797hg38UCSC Ensembl
chr7:110813808..111112853hg19UCSC Ensembl
chr7:110601044..110900089hg18UCSC Ensembl
chr7:110407759..110706804hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38299046
hg19299046
hg18299046
hg17299046
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv519251, nsv528235, nsv527155
Samples
Known GenesIMMP2L
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv427n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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