A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv732809



Internal ID15680079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:192277460..192355045hg38UCSC Ensembl
Innerchr1:192246590..192324175hg19UCSC Ensembl
Innerchr1:190513213..190590798hg18UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg3877586
hg1977586
hg1877586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv548650
Supporting Variants
Samples
Known GenesRGS21
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv732809
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