A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057835



Internal ID19147054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:47061499..47095119hg38UCSC Ensembl
Innerchr22:47457395..47491015hg19UCSC Ensembl
Innerchr22:45836059..45869679hg18UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3833621
hg1933621
hg1833621
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3592268
Samples
Known GenesTBC1D22A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057835
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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