A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696094



Internal ID15432746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:91365454..91501105hg38UCSC Ensembl
Innerchr4:92286605..92422256hg19UCSC Ensembl
Innerchr4:92505628..92641279hg18UCSC Ensembl
Innerchr4:92643783..92779434hg17UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38135652
hg19135652
hg18135652
hg17135652
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518645
Supporting Variants
Samples
Known GenesCCSER1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696094
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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