A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519604



Internal ID15446897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:40834936..40841271hg38UCSC Ensembl
Innerchr4:40836953..40843288hg19UCSC Ensembl
Innerchr4:40531710..40538045hg18UCSC Ensembl
Innerchr4:40677881..40684216hg17UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg386336
hg196336
hg186336
hg176336
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696946
Samples
Known GenesAPBB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519604
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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