A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700073



Internal ID15436725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:152100428..152132694hg38UCSC Ensembl
Innerchr3:151818217..151850483hg19UCSC Ensembl
Innerchr3:153300907..153333173hg18UCSC Ensembl
Innerchr3:153300915..153333181hg17UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3832267
hg1932267
hg1832267
hg1732267
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524190
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700073
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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