A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv904630



Internal ID15851900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:32407596..33072516hg38UCSC Ensembl
Innerchr2:32632664..33297583hg19UCSC Ensembl
Innerchr2:32486168..33151087hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38664921
hg19664920
hg18664920
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581272
Supporting Variants
Samples
Known GenesBIRC6, LINC00486, LOC100271832, LTBP1, MIR4765, MIR558, TTC27
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv904630
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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