A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1003107



Internal ID15950377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:91257564..91332775hg38UCSC Ensembl
Innerchr4:92178715..92253926hg19UCSC Ensembl
Innerchr4:92397738..92472949hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3875212
hg1975212
hg1875212
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594846
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)nssv1003107
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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