A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518247



Internal ID15098854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:36387992..36412515hg38UCSC Ensembl
Innerchr3:36429484..36454007hg19UCSC Ensembl
Innerchr3:36404488..36429011hg18UCSC Ensembl
Innerchr3:36404488..36429011hg17UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3824524
hg1924524
hg1824524
hg1724524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv281n21
Supporting Variantsnssv695678
Samples
Known GenesSTAC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518247
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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