A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv529020



Internal ID15456313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:91332775..91372331hg38UCSC Ensembl
Innerchr4:92253926..92293482hg19UCSC Ensembl
Innerchr4:92472949..92512505hg18UCSC Ensembl
Innerchr4:92611104..92650660hg17UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3839557
hg1939557
hg1839557
hg1739557
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv323n21
Supporting Variantsnssv705731
Samples
Known GenesCCSER1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv529020
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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