A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv928228



Internal ID16222184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:185580666..186002147hg38UCSC Ensembl
Innerchr2:186445393..186866874hg19UCSC Ensembl
Innerchr2:186153638..186575119hg18UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38421482
hg19421482
hg18421482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584019
Supporting Variants
Samples
Known GenesFSIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv928228
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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