A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064489



Internal ID19153708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:29920638..29965892hg38UCSC Ensembl
Innerchr22:30316627..30361881hg19UCSC Ensembl
Innerchr22:28646627..28691881hg18UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg3845255
hg1945255
hg1845255
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3600796, nssv3600795
Samples
Known GenesMTMR3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064489
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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