A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996039



Internal ID15581540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:103650879..103818143hg38UCSC Ensembl
Innerchr8:104663107..104830371hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38167265
hg19167265
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv483082
Supporting Variants
Samples
Known GenesRIMS2
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996039
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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