A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528127



Internal ID15108734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:98225285..98308688hg38UCSC Ensembl
Innerchr4:99146436..99229839hg19UCSC Ensembl
Innerchr4:99365459..99448862hg18UCSC Ensembl
Innerchr4:99503614..99587017hg17UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg3883404
hg1983404
hg1883404
hg1783404
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704672
Samples
Known GenesRAP1GDS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528127
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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