A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669917



Internal ID15059883
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516654
Supporting Variants
Samples
Known GenesACOT11, FAM151A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669917
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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