A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1002841



Internal ID16296797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:90654590..90685238hg38UCSC Ensembl
Innerchr4:91575741..91606389hg19UCSC Ensembl
Innerchr4:91794764..91825412hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3830649
hg1930649
hg1830649
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594832
Supporting Variants
Samples
Known GenesCCSER1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1002841
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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