A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3583008



Internal ID18881289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:167546876..167596377hg38UCSC Ensembl
Innerchr2:168403386..168452887hg19UCSC Ensembl
Innerchr2:168111632..168161133hg18UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3849502
hg1949502
hg1849502
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004326
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3583008
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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