A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv963092



Internal ID15910362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:52501570..52535464hg38UCSC Ensembl
Innerchr3:52535586..52569480hg19UCSC Ensembl
Innerchr3:52510626..52544520hg18UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3833895
hg1933895
hg1833895
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590305
Supporting Variants
Samples
Known GenesNT5DC2, STAB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv963092
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