A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527093



Internal ID15107700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7437531..7439075hg38UCSC Ensembl
Innerchr16:7487532..7489076hg19UCSC Ensembl
Innerchr16:7427533..7429077hg18UCSC Ensembl
Innerchr16:7427533..7429077hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg381545
hg191545
hg181545
hg171545
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703472
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527093
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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