A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062768



Internal ID19151987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:20928403..20947155hg38UCSC Ensembl
Innerchr22:21282691..21301443hg19UCSC Ensembl
Innerchr22:19612691..19631443hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3818753
hg1918753
hg1818753
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4484n100
Supporting Variantsnssv3587385
Samples
Known GenesCRKL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062768
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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