A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524798



Internal ID15452091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:44215170..44221984hg38UCSC Ensembl
Innerchr22:44611050..44617864hg19UCSC Ensembl
Innerchr22:42942383..42949197hg18UCSC Ensembl
Innerchr22:42935951..42942765hg17UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg386815
hg196815
hg186815
hg176815
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv261n21
Supporting Variantsnssv700790
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524798
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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