A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv930557



Internal ID16224513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:203035817..203048829hg38UCSC Ensembl
Innerchr2:203900540..203913552hg19UCSC Ensembl
Innerchr2:203608785..203621797hg18UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg3813013
hg1913013
hg1813013
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584216
Supporting Variants
Samples
Known GenesNBEAL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv930557
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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