A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996248



Internal ID15581749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:116454916..116665498hg38UCSC Ensembl
Innerchr11:116325633..116536215hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38210583
hg19210583
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv483029
Supporting Variants
Samples
Known Genes
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996248
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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