A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv537022



Internal ID15158639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:16809700..16832586hg38UCSC Ensembl
Innerchr3:16851202..16874088hg19UCSC Ensembl
Innerchr3:16826206..16849092hg18UCSC Ensembl
Innerchr3:16826206..16849092hg17UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3822887
hg1922887
hg1822887
hg1722887
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv460454
Supporting Variants
SamplesHGDP00103
Known Genes
MethodSNP array
AnalysisAn HMM examining LogR Ratio and B-allele Frequency was used to classify SNP array data into regions of copy-number 0-3. A combination of manual and automated curation was used on the resulting output to reduce false positives.
PlatformNot reported
Comments
ReferenceItsara_et_al_2009
Pubmed ID19166990
Accession Number(s)nssv537022
Frequency
Sample Size1557
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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