A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521107



Internal ID15101714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:176489248..176499600hg38UCSC Ensembl
Innerchr5:175916249..175926601hg19UCSC Ensembl
Innerchr5:175848855..175859207hg18UCSC Ensembl
Innerchr5:175848855..175859207hg17UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3810353
hg1910353
hg1810353
hg1710353
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694417
Samples
Known GenesFAF2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521107
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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