A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588905



Internal ID16376314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:33360030..33364063hg38UCSC Ensembl
Innerchr22:33756016..33760049hg19UCSC Ensembl
Innerchr22:32086016..32090049hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg384034
hg194034
hg184034
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8085n54
Supporting Variantsnssv954635, nssv954643, nssv954636, nssv954647, nssv954644, nssv954627, nssv954637, nssv954642, nssv954640, nssv954650, nssv954632, nssv954634, nssv954631, nssv954645, nssv954638, nssv954633, nssv954628, nssv954649, nssv954641, nssv954626, nssv954629, nssv954630, nssv954646, nssv954639, nssv954648
Samples
Known GenesLARGE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588905
Frequency
Sample Size17421
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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