A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996093



Internal ID15581594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:177555081..177712521hg38UCSC Ensembl
Innerchr3:177272869..177430309hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38157441
hg19157441
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv482970
Supporting Variants
Samples
Known GenesLINC00578
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996093
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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