A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528008



Internal ID15108615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7163391..7187954hg38UCSC Ensembl
Innerchr16:7213392..7237955hg19UCSC Ensembl
Innerchr16:7153393..7177956hg18UCSC Ensembl
Innerchr16:7153393..7177956hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3824564
hg1924564
hg1824564
hg1724564
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704534
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528008
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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