A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516654



Internal ID15097261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:54580366..54612373hg38UCSC Ensembl
Innerchr1:55046039..55078046hg19UCSC Ensembl
Innerchr1:54818627..54850634hg18UCSC Ensembl
Innerchr1:54758060..54790067hg17UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3832008
hg1932008
hg1832008
hg1732008
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv680692, nssv684126, nssv682791, nssv669917
Samples
Known GenesACOT11, FAM151A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516654
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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