A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv920095



Internal ID15867365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:134103828..134137859hg38UCSC Ensembl
Innerchr2:134861399..134895430hg19UCSC Ensembl
Innerchr2:134577869..134611900hg18UCSC Ensembl
Cytoband2q21.2
Allele length
AssemblyAllele length
hg3834032
hg1934032
hg1834032
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv583170
Supporting Variants
Samples
Known GenesMIR3679
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv920095
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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