A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523547



Internal ID15104154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:36387992..36415880hg38UCSC Ensembl
Innerchr3:36429484..36457372hg19UCSC Ensembl
Innerchr3:36404488..36432376hg18UCSC Ensembl
Innerchr3:36404488..36432376hg17UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3827889
hg1927889
hg1827889
hg1727889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv281n21
Supporting Variantsnssv699325
Samples
Known GenesSTAC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523547
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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