A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525168



Internal ID15105775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:36737010..36745943hg38UCSC Ensembl
Innerchr6:36704787..36713720hg19UCSC Ensembl
Innerchr6:36812765..36821698hg18UCSC Ensembl
Innerchr6:36812765..36821698hg17UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg388934
hg198934
hg188934
hg178934
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv379n21
Supporting Variantsnssv701242
Samples
Known GenesCPNE5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525168
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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