A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv482970



Internal ID15582338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:177555081..177712521hg38UCSC Ensembl
Innerchr3:177272869..177430309hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38157441
hg19157441
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996044, nssv2995928, nssv2996275, nssv2996093, nssv2996235, nssv2996274, nssv2996490, nssv2995956, nssv2996142
Samples
Known GenesLINC00578
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv482970
Frequency
Sample Size39
Observed Gain1
Observed Loss8
Observed Complex0
Frequencyn/a


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