A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522208



Internal ID15449501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:91320436..91362620hg38UCSC Ensembl
Innerchr4:92241587..92283771hg19UCSC Ensembl
Innerchr4:92460610..92502794hg18UCSC Ensembl
Innerchr4:92598765..92640949hg17UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3842185
hg1942185
hg1842185
hg1742185
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv323n21
Supporting Variantsnssv694982
Samples
Known GenesCCSER1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522208
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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