A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521628



Internal ID15448921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:44215170..44221645hg38UCSC Ensembl
Innerchr22:44611050..44617525hg19UCSC Ensembl
Innerchr22:42942383..42948858hg18UCSC Ensembl
Innerchr22:42935951..42942426hg17UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg386476
hg196476
hg186476
hg176476
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv261n21
Supporting Variantsnssv698247
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521628
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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