A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv907332



Internal ID16201288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:41011504..41048432hg38UCSC Ensembl
Innerchr2:41238644..41275572hg19UCSC Ensembl
Innerchr2:41092148..41129076hg18UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3836929
hg1936929
hg1836929
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581567
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv907332
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