A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3600786



Internal ID18899067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:26098646..26110906hg38UCSC Ensembl
Innerchr22:26494612..26506872hg19UCSC Ensembl
Innerchr22:24824612..24836872hg18UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3812261
hg1912261
hg1812261
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057163
Supporting Variants
Samples
Known GenesMIR1302-1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3600786
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer