A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524448



Internal ID15451741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:40980727..40989198hg38UCSC Ensembl
Innerchr4:40982744..40991215hg19UCSC Ensembl
Innerchr4:40677501..40685972hg18UCSC Ensembl
Innerchr4:40823672..40832143hg17UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg388472
hg198472
hg188472
hg178472
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700381
Samples
Known GenesAPBB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524448
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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