A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv957197



Internal ID15904467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:44739898..44741376hg38UCSC Ensembl
Innerchr22:45135778..45137256hg19UCSC Ensembl
Innerchr22:43514442..43515920hg18UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg381479
hg191479
hg181479
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589115
Supporting Variants
Samples
Known GenesPRR5-ARHGAP8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv957197
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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