A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv972942



Internal ID15920212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:127628877..127629589hg38UCSC Ensembl
Innerchr3:127347720..127348432hg19UCSC Ensembl
Innerchr3:128830410..128831122hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38713
hg19713
hg18713
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591582
Supporting Variants
Samples
Known GenesPODXL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv972942
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