A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518229



Internal ID15098836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:83519395..83524112hg38UCSC Ensembl
Innerchr6:84229114..84233831hg19UCSC Ensembl
Innerchr6:84285833..84290550hg18UCSC Ensembl
Innerchr6:84285833..84290550hg17UCSC Ensembl
Cytoband6q14.2
Allele length
AssemblyAllele length
hg384718
hg194718
hg184718
hg174718
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695659
Samples
Known GenesPRSS35
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518229
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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