A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996080



Internal ID15581581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:106011489..106175832hg38UCSC Ensembl
Innerchr10:107771247..107935590hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38164344
hg19164344
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv483107
Supporting Variants
Samples
Known Genes
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996080
Frequency
Sample Size39
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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